Associate, Research Analyst, Industrials, Global Research, Australia
Sydney, New South Wales
Bank of America
Posted 8 days ago
Job Viewed
Job Description
Associate, Research Analyst, Industrials, Global Research, Australia
Sydney, Australia
**To proceed with your application, you must be at least 18 years of age.**
Acknowledge
Refer a friend
**To proceed with your application, you must be at least 18 years of age.**
Acknowledge ( Description:**
At Bank of America, we are guided by a common purpose to help make financial lives better through the power of every connection. We do this by driving Responsible Growth and delivering for our clients, teammates, communities and shareholders every day.
Being a Great Place to Work is core to how we drive Responsible Growth. This includes our commitment to being an inclusive workplace, attracting and developing exceptional talent, supporting our teammates' physical, emotional, and financial wellness, recognizing and rewarding performance, and how we make an impact in the communities we serve.
Bank of America is committed to an in-office culture with specific requirements for office-based attendance and which allows for an appropriate level of flexibility for our teammates and businesses based on role-specific considerations.
At Bank of America, you can build a successful career with opportunities to learn, grow, and make an impact. Join us!
**The Team**
The Australian Equities Research Team focuses on producing high quality and insightful research on listed companies and industry sectors in the Australian region, as well as on global thematic trends impacting sectors under coverage. The team looks to build long-term relationships with, and provide research and analysis to, regional and global institutional investment firms, listed and unlisted companies and key industry players. We require an Associate to join the Australian REITs team.
**The Role**
An opportunity exists for a Research Analyst to join our well rated and dynamic Australian Research team, supporting and being responsible for coverage in the Australian Industrial sector. This role is based in Sydney.
**Responsibilities**
+ Maintain a detailed knowledge of the Australian Industrial companies.
+ Build, maintain and update company models and statistics databases;
+ Writing reports on individual companies and the market sectors;
+ Responding to client requests for data and information;
+ Assisting in the design and preparation of analyst marketing materials;
+ Collaborating with domestic, regional and global colleagues on research projects;
+ Developing relationships and interacting with colleagues in research, equity sales and trading, as well as institutional clients, investor relations, company management and other industry participants;
+ Be responsible for the specific analysis of individual companies and their equities within the Australian Industrial sector;
+ Produce regular reports summarising findings and predictions, as well as responsibility for the sector news flow and contributing to overall sector views/pieces;
+ Develop financial models and interpret data and analysis on market, economic and political events.
**Preferred Background and qualifications/skills**
+ Excellent academic record with a degree in Finance, Accounting or related field;
+ 3-5 years of relevant work experience - preferably in a banking, sell-side equity research, buy-side or utilities/ Industrial related field;
+ Excellent financial modelling skills and a solid grounding in financial/accounting fundamentals;
+ Ability to interpret and analyse company's financial statements, announcements and industry news in order to write research report from the findings;
+ Meticulous attention to detail, self-driven to deliver results and willingness to take responsibility for the outcomes are essential for the role;
+ Highly motivated, proactive, curious and a high level of enthusiasm for equity research;
+ Demonstrated ability to think logically and creatively, generate ideas and exercise good judgment.
Bank of America and its affiliates consider for employment and hire qualified candidates without regard to race, religious creed, religion, color, sex, sexual orientation, genetic information, gender, gender identity, gender expression, age, national origin, ancestry, citizenship, protected veteran or disability status or any factor prohibited by law, and as such affirms in policy and practice to support and promote the concept of equal employment opportunity, in accordance with all applicable federal, state, provincial and municipal laws. The company also prohibits discrimination on other bases such as medical condition, marital status or any other factor that is irrelevant to the performance of our teammates.
To view the "Know your Rights" poster, CLICK HERE ( .
View the LA County Fair Chance Ordinance ( .
Bank of America aims to create a workplace free from the dangers and resulting consequences of illegal and illicit drug use and alcohol abuse. Our Drug-Free Workplace and Alcohol Policy ("Policy") establishes requirements to prevent the presence or use of illegal or illicit drugs or unauthorized alcohol on Bank of America premises and to provide a safe work environment.
To view Bank of America's Drug-free Workplace and Alcohol Policy, CLICK HERE .
Bank of America is committed to an in-office culture with specific requirements for office-based attendance and which allows for an appropriate level of flexibility for our teammates and businesses based on role-specific considerations. Should you be offered a role with Bank of America, your hiring manager will provide you with information on the in-office expectations associated with your role. These expectations are subject to change at any time and at the sole discretion of the Company. To the extent you have a disability or sincerely held religious belief for which you believe you need a reasonable accommodation from this requirement, you must seek an accommodation through the Bank's required accommodation request process before your first day of work.
This communication provides information about certain Bank of America benefits. Receipt of this document does not automatically entitle you to benefits offered by Bank of America. Every effort has been made to ensure the accuracy of this communication. However, if there are discrepancies between this communication and the official plan documents, the plan documents will always govern. Bank of America retains the discretion to interpret the terms or language used in any of its communications according to the provisions contained in the plan documents. Bank of America also reserves the right to amend or terminate any benefit plan in its sole discretion at any time for any reason.
Sydney, Australia
**To proceed with your application, you must be at least 18 years of age.**
Acknowledge
Refer a friend
**To proceed with your application, you must be at least 18 years of age.**
Acknowledge ( Description:**
At Bank of America, we are guided by a common purpose to help make financial lives better through the power of every connection. We do this by driving Responsible Growth and delivering for our clients, teammates, communities and shareholders every day.
Being a Great Place to Work is core to how we drive Responsible Growth. This includes our commitment to being an inclusive workplace, attracting and developing exceptional talent, supporting our teammates' physical, emotional, and financial wellness, recognizing and rewarding performance, and how we make an impact in the communities we serve.
Bank of America is committed to an in-office culture with specific requirements for office-based attendance and which allows for an appropriate level of flexibility for our teammates and businesses based on role-specific considerations.
At Bank of America, you can build a successful career with opportunities to learn, grow, and make an impact. Join us!
**The Team**
The Australian Equities Research Team focuses on producing high quality and insightful research on listed companies and industry sectors in the Australian region, as well as on global thematic trends impacting sectors under coverage. The team looks to build long-term relationships with, and provide research and analysis to, regional and global institutional investment firms, listed and unlisted companies and key industry players. We require an Associate to join the Australian REITs team.
**The Role**
An opportunity exists for a Research Analyst to join our well rated and dynamic Australian Research team, supporting and being responsible for coverage in the Australian Industrial sector. This role is based in Sydney.
**Responsibilities**
+ Maintain a detailed knowledge of the Australian Industrial companies.
+ Build, maintain and update company models and statistics databases;
+ Writing reports on individual companies and the market sectors;
+ Responding to client requests for data and information;
+ Assisting in the design and preparation of analyst marketing materials;
+ Collaborating with domestic, regional and global colleagues on research projects;
+ Developing relationships and interacting with colleagues in research, equity sales and trading, as well as institutional clients, investor relations, company management and other industry participants;
+ Be responsible for the specific analysis of individual companies and their equities within the Australian Industrial sector;
+ Produce regular reports summarising findings and predictions, as well as responsibility for the sector news flow and contributing to overall sector views/pieces;
+ Develop financial models and interpret data and analysis on market, economic and political events.
**Preferred Background and qualifications/skills**
+ Excellent academic record with a degree in Finance, Accounting or related field;
+ 3-5 years of relevant work experience - preferably in a banking, sell-side equity research, buy-side or utilities/ Industrial related field;
+ Excellent financial modelling skills and a solid grounding in financial/accounting fundamentals;
+ Ability to interpret and analyse company's financial statements, announcements and industry news in order to write research report from the findings;
+ Meticulous attention to detail, self-driven to deliver results and willingness to take responsibility for the outcomes are essential for the role;
+ Highly motivated, proactive, curious and a high level of enthusiasm for equity research;
+ Demonstrated ability to think logically and creatively, generate ideas and exercise good judgment.
Bank of America and its affiliates consider for employment and hire qualified candidates without regard to race, religious creed, religion, color, sex, sexual orientation, genetic information, gender, gender identity, gender expression, age, national origin, ancestry, citizenship, protected veteran or disability status or any factor prohibited by law, and as such affirms in policy and practice to support and promote the concept of equal employment opportunity, in accordance with all applicable federal, state, provincial and municipal laws. The company also prohibits discrimination on other bases such as medical condition, marital status or any other factor that is irrelevant to the performance of our teammates.
To view the "Know your Rights" poster, CLICK HERE ( .
View the LA County Fair Chance Ordinance ( .
Bank of America aims to create a workplace free from the dangers and resulting consequences of illegal and illicit drug use and alcohol abuse. Our Drug-Free Workplace and Alcohol Policy ("Policy") establishes requirements to prevent the presence or use of illegal or illicit drugs or unauthorized alcohol on Bank of America premises and to provide a safe work environment.
To view Bank of America's Drug-free Workplace and Alcohol Policy, CLICK HERE .
Bank of America is committed to an in-office culture with specific requirements for office-based attendance and which allows for an appropriate level of flexibility for our teammates and businesses based on role-specific considerations. Should you be offered a role with Bank of America, your hiring manager will provide you with information on the in-office expectations associated with your role. These expectations are subject to change at any time and at the sole discretion of the Company. To the extent you have a disability or sincerely held religious belief for which you believe you need a reasonable accommodation from this requirement, you must seek an accommodation through the Bank's required accommodation request process before your first day of work.
This communication provides information about certain Bank of America benefits. Receipt of this document does not automatically entitle you to benefits offered by Bank of America. Every effort has been made to ensure the accuracy of this communication. However, if there are discrepancies between this communication and the official plan documents, the plan documents will always govern. Bank of America retains the discretion to interpret the terms or language used in any of its communications according to the provisions contained in the plan documents. Bank of America also reserves the right to amend or terminate any benefit plan in its sole discretion at any time for any reason.
This advertiser has chosen not to accept applicants from your region.
0
Senior Research Manager/ Associate Director, Advisors Research Center
St Leonards, New South Wales
Mastercard
Posted 8 days ago
Job Viewed
Job Description
**Our Purpose**
_Mastercard powers economies and empowers people in 200+ countries and territories worldwide. Together with our customers, we're helping build a sustainable economy where everyone can prosper. We support a wide range of digital payments choices, making transactions secure, simple, smart and accessible. Our technology and innovation, partnerships and networks combine to deliver a unique set of products and services that help people, businesses and governments realize their greatest potential._
**Title and Summary**
Senior Research Manager/ Associate Director, Advisors Research Center
Our Purpose
We work to connect and power an inclusive, digital economy that benefits everyone, everywhere by making transactions safe, simple, smart and accessible. Using secure data and networks, partnerships and passion, our innovations and solutions help individuals, financial institutions, governments and businesses realize their greatest potential. Our decency quotient, or DQ, drives our culture and everything we do inside and outside of our company. We cultivate a culture of inclusion for all employees that respects their individual strengths, views, and experiences. We believe that our differences enable us to be a better team - one that makes better decisions, drives innovation and delivers better business results.
All About Us
The Data & Services team is a key differentiator for Mastercard providing the cutting-edge services that help our customers grow. Focused on thinking big and scaling fast around the globe, this agile team is responsible for end-to-end solutions for a diverse global customer base. We combine traditional management consulting with our rich data assets and in-house technology to provide our clients with powerful strategic insights and recommendations. Centered on data-driven technologies and innovation, these services include consulting, loyalty and marketing programs, test-and-learn business experimentation, and data driven information and risk management services. While specializing in the payments industry, Mastercard Data & Services also works closely with major retailers, airlines, and other enterprises, leveraging data and insights garnered from within and beyond its network.
All About the Role
The Advisors Research Center is a global research capability within Mastercard Advisors that responds quickly to evolving customer needs with high-quality research support. With a strong focus on value realization, the Advisors Research Center plays a key role in generating insights and actionable recommendations. It complements and enhances Advisors' traditional strengths, supporting deeper, evidence-based decision-making.
As a Senior Research Manager / Associate Director, you will lead custom research engagements that inform Mastercard's consulting projects, marketing strategies, and product innovations across a wide array of clients and industries.
Your responsibilities would include:
- Lead end-to-end primary research engagements, from proposal and design through to delivery of insights.
- Scope research approaches tailored to strategic business challenges, leveraging qualitative, quantitative, or mixed methods.
- Moderate interviews and focus groups, design surveys, manage vendors, and conduct analysis as needed.
- Synthesize findings into compelling stories with clear, actionable recommendations.
- Mentor junior researchers and contribute to internal capability-building within Advisors Research Center.
All About You
- You are a skilled researcher who is passionate about uncovering insights that matter. You thrive in fast-paced environment and are confident managing multiple projects, stakeholders, and timelines.
- Proven experience leading custom research projects (mainly primary research), ideally in a consultancy, agency, or client-side insights team.
- End-to-end project management capabilities from scoping and design through execution, team oversight and final delivery.
- Strong ability to engage with internal and external stakeholders, including consulting to understand client objectives, frame research questions, and confidently lead presentations and communications throughout the project.
- Experience working with research vendors, including vendor management, managing fieldwork logistics, execution of primary research studies, and questionnaire preparation.
- Demonstrated people management responsibilities, including leading a small team and mentoring junior researchers (preferably, not mandatory).
- Excellent communication and business writing skills, with the ability to translate complex data into clear, compelling insights and produce professional, client-ready materials that influence decision-makers.
All About Your Education & Skills
- 8-10+ years of relevant experience in research, customer insights, or strategy consulting, with a strong emphasis on qualitative research.
- Extensive experience leading primary research projects with a strong focus on qualitative methods, including end-to-end management from design and moderation to analysis and reporting.
- Highly skilled in applying a range of techniques such as in-depth interviews, focus groups, and ethnographic approaches tailored to project objectives and audiences, with a proven ability to generate actionable insights that inform strategic decision-making.
- Preferred (not mandatory) experience in quantitative research methods, with a collaborative mindset to work effectively with quantitative teams and integrate findings for a comprehensive understanding of consumer behavior.
- Strong knowledge of various qualitative research methodologies and tools, with the flexibility to tailor approaches according to specific project objectives and target audiences.
- Familiarity with the financial services industry is preferred, including awareness of recent trends, issues, and key topics.
- Fluency in English is required; proficiency in additional languages is considered an advantage.
- Advanced skills in Microsoft Word, Excel, and PowerPoint are essential, with knowledge of project management tools preferred.
**Corporate Security Responsibility**
All activities involving access to Mastercard assets, information, and networks comes with an inherent risk to the organization and, therefore, it is expected that every person working for, or on behalf of, Mastercard is responsible for information security and must:
+ Abide by Mastercard's security policies and practices;
+ Ensure the confidentiality and integrity of the information being accessed;
+ Report any suspected information security violation or breach, and
+ Complete all periodic mandatory security trainings in accordance with Mastercard's guidelines.
_Mastercard powers economies and empowers people in 200+ countries and territories worldwide. Together with our customers, we're helping build a sustainable economy where everyone can prosper. We support a wide range of digital payments choices, making transactions secure, simple, smart and accessible. Our technology and innovation, partnerships and networks combine to deliver a unique set of products and services that help people, businesses and governments realize their greatest potential._
**Title and Summary**
Senior Research Manager/ Associate Director, Advisors Research Center
Our Purpose
We work to connect and power an inclusive, digital economy that benefits everyone, everywhere by making transactions safe, simple, smart and accessible. Using secure data and networks, partnerships and passion, our innovations and solutions help individuals, financial institutions, governments and businesses realize their greatest potential. Our decency quotient, or DQ, drives our culture and everything we do inside and outside of our company. We cultivate a culture of inclusion for all employees that respects their individual strengths, views, and experiences. We believe that our differences enable us to be a better team - one that makes better decisions, drives innovation and delivers better business results.
All About Us
The Data & Services team is a key differentiator for Mastercard providing the cutting-edge services that help our customers grow. Focused on thinking big and scaling fast around the globe, this agile team is responsible for end-to-end solutions for a diverse global customer base. We combine traditional management consulting with our rich data assets and in-house technology to provide our clients with powerful strategic insights and recommendations. Centered on data-driven technologies and innovation, these services include consulting, loyalty and marketing programs, test-and-learn business experimentation, and data driven information and risk management services. While specializing in the payments industry, Mastercard Data & Services also works closely with major retailers, airlines, and other enterprises, leveraging data and insights garnered from within and beyond its network.
All About the Role
The Advisors Research Center is a global research capability within Mastercard Advisors that responds quickly to evolving customer needs with high-quality research support. With a strong focus on value realization, the Advisors Research Center plays a key role in generating insights and actionable recommendations. It complements and enhances Advisors' traditional strengths, supporting deeper, evidence-based decision-making.
As a Senior Research Manager / Associate Director, you will lead custom research engagements that inform Mastercard's consulting projects, marketing strategies, and product innovations across a wide array of clients and industries.
Your responsibilities would include:
- Lead end-to-end primary research engagements, from proposal and design through to delivery of insights.
- Scope research approaches tailored to strategic business challenges, leveraging qualitative, quantitative, or mixed methods.
- Moderate interviews and focus groups, design surveys, manage vendors, and conduct analysis as needed.
- Synthesize findings into compelling stories with clear, actionable recommendations.
- Mentor junior researchers and contribute to internal capability-building within Advisors Research Center.
All About You
- You are a skilled researcher who is passionate about uncovering insights that matter. You thrive in fast-paced environment and are confident managing multiple projects, stakeholders, and timelines.
- Proven experience leading custom research projects (mainly primary research), ideally in a consultancy, agency, or client-side insights team.
- End-to-end project management capabilities from scoping and design through execution, team oversight and final delivery.
- Strong ability to engage with internal and external stakeholders, including consulting to understand client objectives, frame research questions, and confidently lead presentations and communications throughout the project.
- Experience working with research vendors, including vendor management, managing fieldwork logistics, execution of primary research studies, and questionnaire preparation.
- Demonstrated people management responsibilities, including leading a small team and mentoring junior researchers (preferably, not mandatory).
- Excellent communication and business writing skills, with the ability to translate complex data into clear, compelling insights and produce professional, client-ready materials that influence decision-makers.
All About Your Education & Skills
- 8-10+ years of relevant experience in research, customer insights, or strategy consulting, with a strong emphasis on qualitative research.
- Extensive experience leading primary research projects with a strong focus on qualitative methods, including end-to-end management from design and moderation to analysis and reporting.
- Highly skilled in applying a range of techniques such as in-depth interviews, focus groups, and ethnographic approaches tailored to project objectives and audiences, with a proven ability to generate actionable insights that inform strategic decision-making.
- Preferred (not mandatory) experience in quantitative research methods, with a collaborative mindset to work effectively with quantitative teams and integrate findings for a comprehensive understanding of consumer behavior.
- Strong knowledge of various qualitative research methodologies and tools, with the flexibility to tailor approaches according to specific project objectives and target audiences.
- Familiarity with the financial services industry is preferred, including awareness of recent trends, issues, and key topics.
- Fluency in English is required; proficiency in additional languages is considered an advantage.
- Advanced skills in Microsoft Word, Excel, and PowerPoint are essential, with knowledge of project management tools preferred.
**Corporate Security Responsibility**
All activities involving access to Mastercard assets, information, and networks comes with an inherent risk to the organization and, therefore, it is expected that every person working for, or on behalf of, Mastercard is responsible for information security and must:
+ Abide by Mastercard's security policies and practices;
+ Ensure the confidentiality and integrity of the information being accessed;
+ Report any suspected information security violation or breach, and
+ Complete all periodic mandatory security trainings in accordance with Mastercard's guidelines.
This advertiser has chosen not to accept applicants from your region.
1
Clinical Research Associate 2
North Sydney, New South Wales
IQVIA
Posted 6 days ago
Job Viewed
Job Description
Are you ready to transform lives through Science? We're looking for a Clinical Research Associate in Sydney or Melbourne for our Sponsor-dedicated team. Step into a dynamic role where you'll drive innovation and excellence in clinical research. As a key player in our team, you'll ensure that study sites are not just compliant but thriving, contributing to groundbreaking advancements in healthcare. Your work fuels the future of healthcare.
When you join IQVIA AUSTRALIA as a sponsor-dedicated CRA, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
With access to world-class training and mentoring, you'll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
You must have a minimum of 18 months Independent on-site monitoring experience to be considered for this role. We regret to inform you that we can not consider sponsorship for this role at this stage so only candidates with full work rights will be contacted.
You will be asked to complete a short video screening as part of the interview process.
Sydney and Melbourne are preferred locations.
**Essential Functions:**
+ **Engage in Site Visits:** From selection to close-out, your visits will be pivotal in ensuring the success of our studies.
+ **Recruitment Strategies:** Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes
+ **Empower Sites with Knowledge:** Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
+ **Champion Quality and Integrity:** Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
+ **Drive Study Progress:** Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.
+ **Master Documentation:** Keep meticulous records and ensure all site documents are perfectly maintained.
+ **Collaborate and Innovate:** Work closely with a passionate team to support project execution and drive success.
+ **Manage Finances with Precision:** Oversee site financials and ensure timely invoice retrieval.
**Qualifications:**
+ **Educational Excellence:** Bachelor's degree in a scientific or healthcare discipline preferred.
+ **Experience Matters:** At least 18 months of on-site monitoring experience (across Australia), with preference for Oncology and Haematology trial management exposure.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
When you join IQVIA AUSTRALIA as a sponsor-dedicated CRA, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
With access to world-class training and mentoring, you'll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
You must have a minimum of 18 months Independent on-site monitoring experience to be considered for this role. We regret to inform you that we can not consider sponsorship for this role at this stage so only candidates with full work rights will be contacted.
You will be asked to complete a short video screening as part of the interview process.
Sydney and Melbourne are preferred locations.
**Essential Functions:**
+ **Engage in Site Visits:** From selection to close-out, your visits will be pivotal in ensuring the success of our studies.
+ **Recruitment Strategies:** Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes
+ **Empower Sites with Knowledge:** Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
+ **Champion Quality and Integrity:** Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
+ **Drive Study Progress:** Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.
+ **Master Documentation:** Keep meticulous records and ensure all site documents are perfectly maintained.
+ **Collaborate and Innovate:** Work closely with a passionate team to support project execution and drive success.
+ **Manage Finances with Precision:** Oversee site financials and ensure timely invoice retrieval.
**Qualifications:**
+ **Educational Excellence:** Bachelor's degree in a scientific or healthcare discipline preferred.
+ **Experience Matters:** At least 18 months of on-site monitoring experience (across Australia), with preference for Oncology and Haematology trial management exposure.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
2
Research Assistant-Protein Science
Sydney, New South Wales
Teva Pharmaceuticals
Posted 8 days ago
Job Viewed
Job Description
Research Assistant-Protein Science
Date: Jul 2, 2025
Location:
Sydney, Australia, -
Company: Teva Pharmaceuticals
Job Id: 62673
**Who we are**
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
**The opportunity**
We are currently seeking a driven and detail-oriented Research Assistant specializing in Protein Science to join our team on a parental leave contract running through to June 2026.
We are looking for someone who brings enthusiasm, scientific curiosity, strong attention to detail, someone who thrives in a fast-paced setting. This is a rare opportunity to contribute to cutting edge projects in a collaborative and forward-thinking environment.
In this role, you will plan and conduct cell culture experiments, perform protein purification, and conduct biophysical characterization of proteins to enable research and development of novel biologic therapeutics.
**How you'll spend your day**
- Assist in the design, planning, and execution of research projects focused on protein science.
- Generating and characterizing proteins including the following responsibilities: General molecular biology, and DNA preparation.
- Mammalian cell culture for recombinant protein expression.
- Lab scale method development for antibody and target protein purification.
- Collect, analyse, and interpret experimental data, ensuring accuracy and reliability.
- Maintain detailed records of experiments, protocols, and results.
- Collaborate with senior researchers and cross-functional teams to support ongoing projects and initiatives.
- Contribute to the preparation of research reports, publications, and presentations.
- Stay current with the latest scientific advancements and techniques in protein science.
- Ensure compliance with all relevant safety, environmental, and regulatory standards.
- Maintain laboratory equipment and inventory, ensuring a clean and organized work environment.
**Your experience and qualifications**
- Bachelor's degree in Life sciences with an honour's degree
- Experience in protein analysis and characterization techniques
- Experience in mammalian cell culture, protein purification by liquid chromatography and analytical characterization methods
- Strong analytical and problem-solving skills
- Excellent attention to detail and organizational skills
- Proficiency in using laboratory instruments and software for data analysis
- Strong communication and interpersonal skills
- Ability to work independently and as part of a team in a fast-paced, dynamic environment
**Enjoy a more rewarding choice**
- Work with a motivated team of scientists in state-of-the-art laboratories
- Generous leave, health, and wellbeing benefits
- Parking available at our Macquarie Park site
- Opportunity to join a leading global organisation with a network of 37,000 employees operating in 60 markets, with 25 R&D sites
**Make a difference with Teva Pharmaceuticals**
Please submit your CV and a Cover Letter.
Please note that only shortlisted candidates will be contacted.
**Reports To**
Senior Research Scientist
**Already Working @TEVA?**
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:Internal Career Site ( internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
EOE including disability/veteran
Date: Jul 2, 2025
Location:
Sydney, Australia, -
Company: Teva Pharmaceuticals
Job Id: 62673
**Who we are**
Together, we're on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It's a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world's leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization's Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we're always looking for new ways to continue making a difference, and new people to make a difference with.
**The opportunity**
We are currently seeking a driven and detail-oriented Research Assistant specializing in Protein Science to join our team on a parental leave contract running through to June 2026.
We are looking for someone who brings enthusiasm, scientific curiosity, strong attention to detail, someone who thrives in a fast-paced setting. This is a rare opportunity to contribute to cutting edge projects in a collaborative and forward-thinking environment.
In this role, you will plan and conduct cell culture experiments, perform protein purification, and conduct biophysical characterization of proteins to enable research and development of novel biologic therapeutics.
**How you'll spend your day**
- Assist in the design, planning, and execution of research projects focused on protein science.
- Generating and characterizing proteins including the following responsibilities: General molecular biology, and DNA preparation.
- Mammalian cell culture for recombinant protein expression.
- Lab scale method development for antibody and target protein purification.
- Collect, analyse, and interpret experimental data, ensuring accuracy and reliability.
- Maintain detailed records of experiments, protocols, and results.
- Collaborate with senior researchers and cross-functional teams to support ongoing projects and initiatives.
- Contribute to the preparation of research reports, publications, and presentations.
- Stay current with the latest scientific advancements and techniques in protein science.
- Ensure compliance with all relevant safety, environmental, and regulatory standards.
- Maintain laboratory equipment and inventory, ensuring a clean and organized work environment.
**Your experience and qualifications**
- Bachelor's degree in Life sciences with an honour's degree
- Experience in protein analysis and characterization techniques
- Experience in mammalian cell culture, protein purification by liquid chromatography and analytical characterization methods
- Strong analytical and problem-solving skills
- Excellent attention to detail and organizational skills
- Proficiency in using laboratory instruments and software for data analysis
- Strong communication and interpersonal skills
- Ability to work independently and as part of a team in a fast-paced, dynamic environment
**Enjoy a more rewarding choice**
- Work with a motivated team of scientists in state-of-the-art laboratories
- Generous leave, health, and wellbeing benefits
- Parking available at our Macquarie Park site
- Opportunity to join a leading global organisation with a network of 37,000 employees operating in 60 markets, with 25 R&D sites
**Make a difference with Teva Pharmaceuticals**
Please submit your CV and a Cover Letter.
Please note that only shortlisted candidates will be contacted.
**Reports To**
Senior Research Scientist
**Already Working @TEVA?**
If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply:Internal Career Site ( internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.
**Teva's Equal Employment Opportunity Commitment**
Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.
EOE including disability/veteran
This advertiser has chosen not to accept applicants from your region.
3
(Senior) Clinical Research Associate
North Sydney, New South Wales
IQVIA
Posted 8 days ago
Job Viewed
Job Description
Are you ready to transform lives through Science? We're looking for a Clinical Research Associate in Sydney or Melbourne for our Sponsor-dedicated team. Step into a dynamic role where you'll drive innovation and excellence in clinical research. As a key player in our team, you'll ensure that study sites are not just compliant but thriving, contributing to groundbreaking advancements in healthcare. Your work fuels the future of healthcare.
When you join IQVIA AUSTRALIA as a sponsor-dedicated CRA, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
With access to world-class training and mentoring, you'll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
You must have a minimum of 18 months Independent on-site monitoring experience to be considered for a CRA 2 role and a minimum of 4 years independent on-site monitoring experience to be considered as a Senior. We regret to inform you that we can not consider sponsorship for this role at this stage so only candidates with full work rights will be contacted.
You will be asked to complete a short video screening as part of the interview process.
**Essential Functions:**
+ **Engage in Site Visits:** From selection to close-out, your visits will be pivotal in ensuring the success of our studies.
+ **Recruitment Strategies:** Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes
+ **Empower Sites with Knowledge:** Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
+ **Champion Quality and Integrity:** Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
+ **Drive Study Progress:** Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.
+ **Master Documentation:** Keep meticulous records and ensure all site documents are perfectly maintained.
+ **Collaborate and Innovate:** Work closely with a passionate team to support project execution and drive success.
+ **Manage Finances with Precision:** Oversee site financials and ensure timely invoice retrieval.
**Qualifications:**
+ **Educational Excellence:** Bachelor's degree in a scientific or healthcare discipline preferred.
+ **Experience Matters:** At least 18 months of on-site monitoring experience (across Australia), with preference for Oncology and/or Hematology trial management exposure.
+ **Regulatory Savvy:** Strong knowledge of GCP and ICH guidelines.
+ **Tech-Savvy:** Proficiency in Microsoft Office and relevant technology.
+ **Communication Pro:** Excellent written and verbal skills.
+ **Organized and Analytical:** Strong organizational and problem-solving abilities.
+ **Time and Financial Management:** Effective in managing time and finances.
+ **Team Player:** Ability to build and maintain strong relationships with coworkers, managers, and clients.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
When you join IQVIA AUSTRALIA as a sponsor-dedicated CRA, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers.
With access to world-class training and mentoring, you'll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
You must have a minimum of 18 months Independent on-site monitoring experience to be considered for a CRA 2 role and a minimum of 4 years independent on-site monitoring experience to be considered as a Senior. We regret to inform you that we can not consider sponsorship for this role at this stage so only candidates with full work rights will be contacted.
You will be asked to complete a short video screening as part of the interview process.
**Essential Functions:**
+ **Engage in Site Visits:** From selection to close-out, your visits will be pivotal in ensuring the success of our studies.
+ **Recruitment Strategies:** Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes
+ **Empower Sites with Knowledge:** Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
+ **Champion Quality and Integrity:** Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
+ **Drive Study Progress:** Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.
+ **Master Documentation:** Keep meticulous records and ensure all site documents are perfectly maintained.
+ **Collaborate and Innovate:** Work closely with a passionate team to support project execution and drive success.
+ **Manage Finances with Precision:** Oversee site financials and ensure timely invoice retrieval.
**Qualifications:**
+ **Educational Excellence:** Bachelor's degree in a scientific or healthcare discipline preferred.
+ **Experience Matters:** At least 18 months of on-site monitoring experience (across Australia), with preference for Oncology and/or Hematology trial management exposure.
+ **Regulatory Savvy:** Strong knowledge of GCP and ICH guidelines.
+ **Tech-Savvy:** Proficiency in Microsoft Office and relevant technology.
+ **Communication Pro:** Excellent written and verbal skills.
+ **Organized and Analytical:** Strong organizational and problem-solving abilities.
+ **Time and Financial Management:** Effective in managing time and finances.
+ **Team Player:** Ability to build and maintain strong relationships with coworkers, managers, and clients.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
4
Site Research Assistant - Condord
North Sydney, New South Wales
IQVIA
Posted 8 days ago
Job Viewed
Job Description
Are you looking for an opportunity to work with an industry-leading company? IQVIA is currently recruiting for a Clinical Research Coordinator to support a site in Concord.
This role with an immediate start is for **8** **hours** per week and is expected to last around one year. Working day will be Friday.
The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including:
+ Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
+ Support with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.);
+ Planning and coordinating logistical activity for study procedures according to the study protocol
+ Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
+ Management and shipment of biological samples
+ Performing ECG, taking vital signs, phlebotomy
+ Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions
+ Administrative research task
We are looking for candidates with:
+ BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession
+ Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
+ **Must have at least 2 years experience working as a Clinical Research Assistant or Clinical Research Coordinator at a clinical trial site**
+ Basic knowledge of medical terminology
+ Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
+ Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
+ Good organizational skills with the ability to pay close attention to detail
?If this sounds like the perfect opportunity for you, please apply now!
#LI-CES
#LI-NS1
#LI-HCPN
#LI-DNP
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This role with an immediate start is for **8** **hours** per week and is expected to last around one year. Working day will be Friday.
The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies, under the direction and delegation of the Principal Investigator.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support the clinical trial team and ensure the smooth running of the clinical trial, including:
+ Maintaining up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
+ Support with screening and enrolment of patients and collection of related documents (informed consent, privacy consent, etc.);
+ Planning and coordinating logistical activity for study procedures according to the study protocol
+ Data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
+ Management and shipment of biological samples
+ Performing ECG, taking vital signs, phlebotomy
+ Coordinating with study monitor on study issues and effectively responding to monitor-initiated questions
+ Administrative research task
We are looking for candidates with:
+ BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, Research Assistant, nurse, medical assistant, other medical profession
+ Good knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
+ **Must have at least 2 years experience working as a Clinical Research Assistant or Clinical Research Coordinator at a clinical trial site**
+ Basic knowledge of medical terminology
+ Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
+ Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and clients
+ Good organizational skills with the ability to pay close attention to detail
?If this sounds like the perfect opportunity for you, please apply now!
#LI-CES
#LI-NS1
#LI-HCPN
#LI-DNP
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate 2
North Sydney, New South Wales
IQVIA
Posted 8 days ago
Job Viewed
Job Description
Are you passionate about science, driven by purpose, and ready to make a real impact in the world of clinical research? We're looking for a Clinical Research Associate 2 who's ready to take their career to the next level-working on cutting-edge studies that shape the future of medicine. Ideally Sydney or Melbourne. We can not consider sponsorship for this role so please only apply if you currently hold full work rights to work in Australia.
Please note as part of the assessment you will be asked for complete a short video screening interview.
Essential Functions:
+ Engage in Site Visits: From selection to close-out, your visits will be pivotal in ensuring the success of our studies.
+ Recruitment Strategies: Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes
+ Empower Sites with Knowledge: Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
+ Champion Quality and Integrity: Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
+ Drive Study Progress: Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.
+ Master Documentation: Keep meticulous records and ensure all site documents are perfectly maintained.
+ Collaborate and Innovate: Work closely with a passionate team to support project execution and drive success.
+ Manage Finances with Precision: Oversee site financials and ensure timely invoice retrieval.
**What You Bring**
+ A degree in life sciences or healthcare (or equivalent experience).
+ 18 months minimum of on-site monitoring experience to be considered ideally oncology
+ Deep knowledge of GCP, ICH, and clinical trial operations.
+ Tech-savvy with Microsoft Office and mobile tools (iPhone/iPad).
+ A proactive mindset, strong communication skills, and a passion for excellence.
**Why Join Us?**
+ Work ondiverse, global studiesacross multiple therapeutic areas.
+ Be part of asupportive, innovative teamthat values your growth.
+ Enjoyflexible work arrangements, travel opportunities, and career develop
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
Please note as part of the assessment you will be asked for complete a short video screening interview.
Essential Functions:
+ Engage in Site Visits: From selection to close-out, your visits will be pivotal in ensuring the success of our studies.
+ Recruitment Strategies: Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes
+ Empower Sites with Knowledge: Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
+ Champion Quality and Integrity: Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
+ Drive Study Progress: Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.
+ Master Documentation: Keep meticulous records and ensure all site documents are perfectly maintained.
+ Collaborate and Innovate: Work closely with a passionate team to support project execution and drive success.
+ Manage Finances with Precision: Oversee site financials and ensure timely invoice retrieval.
**What You Bring**
+ A degree in life sciences or healthcare (or equivalent experience).
+ 18 months minimum of on-site monitoring experience to be considered ideally oncology
+ Deep knowledge of GCP, ICH, and clinical trial operations.
+ Tech-savvy with Microsoft Office and mobile tools (iPhone/iPad).
+ A proactive mindset, strong communication skills, and a passion for excellence.
**Why Join Us?**
+ Work ondiverse, global studiesacross multiple therapeutic areas.
+ Be part of asupportive, innovative teamthat values your growth.
+ Enjoyflexible work arrangements, travel opportunities, and career develop
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
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6
Senior Clinical Research Associate
North Sydney, New South Wales
IQVIA
Posted 8 days ago
Job Viewed
Job Description
Currently seeking Senior Clinical Research Associate for our Sponsor-dedicated team. Step into a dynamic role where you'll drive innovation and excellence in clinical research. As a key player in our team, you'll ensure that study sites are not just compliant but thriving, contributing to groundbreaking advancements in healthcare.
When you join IQVIA AUSTRALIA as a sponsor-dedicated CRA, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. With access to world-class training and mentoring, you'll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
You must have a minimum of 4 years Independent on-site monitoring experience to be considered for this role. We regret to inform you that we can not consider sponsorship for this role at this stage so only candidates with full work rights will be contacted.
You will be asked to complete a short video screening as part of the interview process.
Sydney and Melbourne are preferred locations for this role.
**Essential Functions:**
+ Engage in Site Visits: From selection to close-out, your visits will be pivotal in ensuring the success of our studies.
+ Recruitment Strategies: Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes
+ Empower Sites with Knowledge: Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
+ Champion Quality and Integrity: Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
+ Drive Study Progress: Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.
+ Master Documentation: Keep meticulous records and ensure all site documents are perfectly maintained.
+ Collaborate and Innovate: Work closely with a passionate team to support project execution and drive success.
+ Manage Finances with Precision: Oversee site financials and ensure timely invoice retrieval.
**Qualifications:**
+ Educational Excellence: Bachelor's degree in a scientific or healthcare discipline preferred.
+ Experience Matters: At least 4 years of on-site monitoring experience (across Australia), with preference for Oncology trial management exposure.
+ Regulatory Savvy: Strong knowledge of GCP and ICH guidelines.
+ Tech-Savvy: Proficiency in Microsoft Office and relevant technology.
+ Communication Pro: Excellent written and verbal skills.
+ Organized and Analytical: Strong organizational and problem-solving abilities.
+ Time and Financial Management: Effective in managing time and finances.
+ Team Player: Ability to build and maintain strong relationships with coworkers, managers, and clients.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
When you join IQVIA AUSTRALIA as a sponsor-dedicated CRA, you'll enjoy the stability and resources of a leading, global contract research organization while gaining direct experience with one of our customers. With access to world-class training and mentoring, you'll have the opportunity to put your passions to work in an environment designed to help you gain experience in a wide variety of therapeutic areas.
You must have a minimum of 4 years Independent on-site monitoring experience to be considered for this role. We regret to inform you that we can not consider sponsorship for this role at this stage so only candidates with full work rights will be contacted.
You will be asked to complete a short video screening as part of the interview process.
Sydney and Melbourne are preferred locations for this role.
**Essential Functions:**
+ Engage in Site Visits: From selection to close-out, your visits will be pivotal in ensuring the success of our studies.
+ Recruitment Strategies: Develop and implement innovative plans to recruit study subjects, making a tangible impact on project outcomes
+ Empower Sites with Knowledge: Provide essential training and maintain robust communication channels to keep sites aligned and motivated.
+ Champion Quality and Integrity: Evaluate and enhance site practices, ensuring adherence to protocols and regulations.
+ Drive Study Progress: Monitor every aspect of the study, from regulatory submissions to data query resolutions, ensuring seamless execution.
+ Master Documentation: Keep meticulous records and ensure all site documents are perfectly maintained.
+ Collaborate and Innovate: Work closely with a passionate team to support project execution and drive success.
+ Manage Finances with Precision: Oversee site financials and ensure timely invoice retrieval.
**Qualifications:**
+ Educational Excellence: Bachelor's degree in a scientific or healthcare discipline preferred.
+ Experience Matters: At least 4 years of on-site monitoring experience (across Australia), with preference for Oncology trial management exposure.
+ Regulatory Savvy: Strong knowledge of GCP and ICH guidelines.
+ Tech-Savvy: Proficiency in Microsoft Office and relevant technology.
+ Communication Pro: Excellent written and verbal skills.
+ Organized and Analytical: Strong organizational and problem-solving abilities.
+ Time and Financial Management: Effective in managing time and finances.
+ Team Player: Ability to build and maintain strong relationships with coworkers, managers, and clients.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
7
Director, Clinical Research & Market Access APAC
St Leonards, New South Wales
Stryker
Posted 8 days ago
Job Viewed
Job Description
**Who We Are Looking For:**
**Sets direction.** An innovator who defines ways to create value and deliver on Stryker's mission and strategic imperatives.
**Builds organizational capability.** A strategic executive who continuously breaks down barriers, identifying new and more effective ways to accomplish tasks and goals.
**Inspires others.** A genuine, relationship-focused leader who connects, collaborates and fosters an inclusive environment of enthusiasm, trust and pride. He/she makes others want to follow, building momentum for action and positively influencing outcomes.
The **Director Clinical Research & Market Access, APAC** will lead, develop and execute market access and clinical research activities across the Asia-Pacific region, aligning with the strategic direction and priorities for the Orthopaedics, Spine & Digital portfolio.
This position can be based in Singapore or Sydney, Australia.
**The Role**
+ To champion the needs of APAC with division ensuring key research needs are understood and incorporated into division commercial planning. To develop and coordinate an APAC wide research strategy that will communicate the economic and clinical value Stryker products can deliver across the APAC healthcare environment.
+ Coordination, Development and Execution of research plans that ensure Orthopaedics, Spine & digital is conducting the right research at the right cadence to support the business's growth expectations across the region, and develop research KOLs to deliver a strong podium and publication presence across the region and globally.
+ Accelerate the speed to market for products in APAC, and maximise reimbursement opportunities in collaboration with Regulatory and commercial leaders.
+ Internal Partnership with legal, compliance, commercial and division to ensure APAC can gain market access to current and future digital infrastructure, products and services.
+ To be a Clinical research and market access talent / brand ambassador, building key productive relationship with key educational institutes outside of Stryker and enhance clinical and reimbursement capabilities across the APAC region.
+ With a primary focus on Japan, SSP and China, while developing capabilities in the markets of India and East Asia, work closely with the regional marketing leadership, local GMs, business leaders and marketing teams to drive growth, align divisional and regional needs and execute, coordinate, support, and supplement relevant commercial activities in the region.
+ Act as an interface/bridge in the business to foster increased regional synergy and promote APAC needs, clinical and business opportunities of the region to division. Influencing and selling the power and potential of APAC to division and fostering divisional collaboration and regional representation on priority Orthopaedic, Spine & Digital portfolio programs.
+ Create an APAC clinical research leadership group to ensure local research activity is shared, all activity and research is visible and each trial delivers the maximum value to the region. While creating a clear podium plan for the regions key events to effectively communicate the value Stryker products can bring to APAC customers.
+ Visit local/regional teams to proactively identify and support business opportunities and gain market insights through VOC with local customers, and KOLs, to help develop and execute market access and clinical research activities.
+ Develop and maintain the 5-10yr market access, reimbursement and clinical research roadmap strategy/plan for the region across the Orthopaedic, Spine & Digital businesses. Including required investments, resources and impact / metrics estimates. Partner with division, and APAC RAQA, reimbursement, commercial and marketing teams to accelerate speed to market for products aligned to strategic growth segments / strategies.
+ Support the development and build the capability of the APAC reimbursement and clinical research teams in country, by driving a focus on increasing go to market / clinical research excellence in the region, and contributing to, commercialization plans and products launch execution.
**_Key areas of accountability:_**
+ Develop and grow our clinical research capabilities and accelerate market access and reimbursement in Asia Pacific
+ Responsible for designing and effective execution of the clinical research strategy for Orthopaedics, Spine & Digital. Establishing thought leadership in key segments where Stryker can lead thought leadership.
+ Working closely with market leadership teams to develop a clear clinical research strategy - these clinical studies should aid insights to overcome customer objections, demonstrate the clinical and economic value and maximise reimbursement of Stryker's products and services.
+ Develop a regional KOL network and build strong, trusted and influential relationships with these KOL's facilitating research, podium and publication strategies that are well planned and co-ordinated to drive thought leadership across the region for portfolio priorities and identified must win segments.
+ Establish and maintain strong, productive relationships with Universities, governments and other key health and technical organizations/thought leaders outside of Stryker.
+ Play an active role in APAC product launch teams for key priority products to accelerate market access and maximise reimbursement and the growth impact of product launches across APAC by driving enhanced clinical programs.
+ Ensuring Stryker has a resonating economic, value based health proposition for key Digital, Robotic and Enabling technologies today and into the future to demonstrate enhanced clinical outcomes and economic savings across healthcare markets in APAC.
+ Provide a clinical and reimbursement coordination across the Asia Pacific Markets and link with Product Divisions.
+ Collaborate and influence Division on global clinical strategies and develop specific market access and reimbursement plans for the key markets when needed. Partner with division to coordinate pre-commercialization / commercialization plan inputs to accelerate product access for Asia Pacific. Build trust and understanding with APAC markets to forge stronger relationships with division.
+ Be the point of contact for Asia Pacific for all OST clinical research and reimbursement related communication and activities. Ensuring that there are robust processes in place to share communications with markets across the region when relevant, to ensure research output is maximized and not duplicated
+ Collaborate with markets to develop and maintain a 5-10 year APAC wide clinical research and reimbursement roadmap.
+ Collaborate with markets to develop and maintain an APAC wide clinical research institute and KOL map, understanding unique and or specialized capabilities each can deliver.
+ Team Development
+ Provide direction, mentorship and development on clinical research, market access and reimbursement to required teams and customers across the APAC business.
+ Increase ambition and hold teams accountable to clinical research and reimbursement excellence, utilizing and coaching on Stryker frameworks
+ Promote a culture of integrity and achievement and lead the team to success with consistent reference to Stryker values
+ Work with regulatory teams on OST & Digital regulatory strategy and ensure support from division with timely provision of required product information, to accelerate speed to market.
+ Understand the data capture, management and transfer landscape, laws and regulations with respect to digital and data handling in the region, including informed consent and build out a growth plan for the region in order for Stryker to develop and accelerate scalable data intelligence and real world evidence collection to drive added clinical and economic value for our products and services across APAC markets.
**The Candidate**
+ Bachelor or Masters or PhD degree in scientific field, preferably in, Engineering, Science or in a relevant scientific field.
+ At least 10+ years of relevant clinical experience, with proven track record of success at a senior level.
+ Extensive experience within the Orthopaedics and Spine fields strongly preferred
+ Strong knowledge and application of clinical trial design, governance and publication pathways.
+ Expertise in developing clinical research plans in conjunction with marketing partners and driving clinical excellence across stakeholders both internally and externally.
+ High level capability in KOL management and development, with focus in clinical research, research execution, manuscript development, podium planning.
+ influencing ability across stakeholders of various cultures and seniority levels,
+ Demonstrated ability to work with multi-discipline, multi-technology teams to drive delivery of research and market access plans
+ Ability to build relationships across the organization and work with different cultures
+ Highly capable to manage complex projects, be strategic and have excellent planning and execution skills
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
**Sets direction.** An innovator who defines ways to create value and deliver on Stryker's mission and strategic imperatives.
**Builds organizational capability.** A strategic executive who continuously breaks down barriers, identifying new and more effective ways to accomplish tasks and goals.
**Inspires others.** A genuine, relationship-focused leader who connects, collaborates and fosters an inclusive environment of enthusiasm, trust and pride. He/she makes others want to follow, building momentum for action and positively influencing outcomes.
The **Director Clinical Research & Market Access, APAC** will lead, develop and execute market access and clinical research activities across the Asia-Pacific region, aligning with the strategic direction and priorities for the Orthopaedics, Spine & Digital portfolio.
This position can be based in Singapore or Sydney, Australia.
**The Role**
+ To champion the needs of APAC with division ensuring key research needs are understood and incorporated into division commercial planning. To develop and coordinate an APAC wide research strategy that will communicate the economic and clinical value Stryker products can deliver across the APAC healthcare environment.
+ Coordination, Development and Execution of research plans that ensure Orthopaedics, Spine & digital is conducting the right research at the right cadence to support the business's growth expectations across the region, and develop research KOLs to deliver a strong podium and publication presence across the region and globally.
+ Accelerate the speed to market for products in APAC, and maximise reimbursement opportunities in collaboration with Regulatory and commercial leaders.
+ Internal Partnership with legal, compliance, commercial and division to ensure APAC can gain market access to current and future digital infrastructure, products and services.
+ To be a Clinical research and market access talent / brand ambassador, building key productive relationship with key educational institutes outside of Stryker and enhance clinical and reimbursement capabilities across the APAC region.
+ With a primary focus on Japan, SSP and China, while developing capabilities in the markets of India and East Asia, work closely with the regional marketing leadership, local GMs, business leaders and marketing teams to drive growth, align divisional and regional needs and execute, coordinate, support, and supplement relevant commercial activities in the region.
+ Act as an interface/bridge in the business to foster increased regional synergy and promote APAC needs, clinical and business opportunities of the region to division. Influencing and selling the power and potential of APAC to division and fostering divisional collaboration and regional representation on priority Orthopaedic, Spine & Digital portfolio programs.
+ Create an APAC clinical research leadership group to ensure local research activity is shared, all activity and research is visible and each trial delivers the maximum value to the region. While creating a clear podium plan for the regions key events to effectively communicate the value Stryker products can bring to APAC customers.
+ Visit local/regional teams to proactively identify and support business opportunities and gain market insights through VOC with local customers, and KOLs, to help develop and execute market access and clinical research activities.
+ Develop and maintain the 5-10yr market access, reimbursement and clinical research roadmap strategy/plan for the region across the Orthopaedic, Spine & Digital businesses. Including required investments, resources and impact / metrics estimates. Partner with division, and APAC RAQA, reimbursement, commercial and marketing teams to accelerate speed to market for products aligned to strategic growth segments / strategies.
+ Support the development and build the capability of the APAC reimbursement and clinical research teams in country, by driving a focus on increasing go to market / clinical research excellence in the region, and contributing to, commercialization plans and products launch execution.
**_Key areas of accountability:_**
+ Develop and grow our clinical research capabilities and accelerate market access and reimbursement in Asia Pacific
+ Responsible for designing and effective execution of the clinical research strategy for Orthopaedics, Spine & Digital. Establishing thought leadership in key segments where Stryker can lead thought leadership.
+ Working closely with market leadership teams to develop a clear clinical research strategy - these clinical studies should aid insights to overcome customer objections, demonstrate the clinical and economic value and maximise reimbursement of Stryker's products and services.
+ Develop a regional KOL network and build strong, trusted and influential relationships with these KOL's facilitating research, podium and publication strategies that are well planned and co-ordinated to drive thought leadership across the region for portfolio priorities and identified must win segments.
+ Establish and maintain strong, productive relationships with Universities, governments and other key health and technical organizations/thought leaders outside of Stryker.
+ Play an active role in APAC product launch teams for key priority products to accelerate market access and maximise reimbursement and the growth impact of product launches across APAC by driving enhanced clinical programs.
+ Ensuring Stryker has a resonating economic, value based health proposition for key Digital, Robotic and Enabling technologies today and into the future to demonstrate enhanced clinical outcomes and economic savings across healthcare markets in APAC.
+ Provide a clinical and reimbursement coordination across the Asia Pacific Markets and link with Product Divisions.
+ Collaborate and influence Division on global clinical strategies and develop specific market access and reimbursement plans for the key markets when needed. Partner with division to coordinate pre-commercialization / commercialization plan inputs to accelerate product access for Asia Pacific. Build trust and understanding with APAC markets to forge stronger relationships with division.
+ Be the point of contact for Asia Pacific for all OST clinical research and reimbursement related communication and activities. Ensuring that there are robust processes in place to share communications with markets across the region when relevant, to ensure research output is maximized and not duplicated
+ Collaborate with markets to develop and maintain a 5-10 year APAC wide clinical research and reimbursement roadmap.
+ Collaborate with markets to develop and maintain an APAC wide clinical research institute and KOL map, understanding unique and or specialized capabilities each can deliver.
+ Team Development
+ Provide direction, mentorship and development on clinical research, market access and reimbursement to required teams and customers across the APAC business.
+ Increase ambition and hold teams accountable to clinical research and reimbursement excellence, utilizing and coaching on Stryker frameworks
+ Promote a culture of integrity and achievement and lead the team to success with consistent reference to Stryker values
+ Work with regulatory teams on OST & Digital regulatory strategy and ensure support from division with timely provision of required product information, to accelerate speed to market.
+ Understand the data capture, management and transfer landscape, laws and regulations with respect to digital and data handling in the region, including informed consent and build out a growth plan for the region in order for Stryker to develop and accelerate scalable data intelligence and real world evidence collection to drive added clinical and economic value for our products and services across APAC markets.
**The Candidate**
+ Bachelor or Masters or PhD degree in scientific field, preferably in, Engineering, Science or in a relevant scientific field.
+ At least 10+ years of relevant clinical experience, with proven track record of success at a senior level.
+ Extensive experience within the Orthopaedics and Spine fields strongly preferred
+ Strong knowledge and application of clinical trial design, governance and publication pathways.
+ Expertise in developing clinical research plans in conjunction with marketing partners and driving clinical excellence across stakeholders both internally and externally.
+ High level capability in KOL management and development, with focus in clinical research, research execution, manuscript development, podium planning.
+ influencing ability across stakeholders of various cultures and seniority levels,
+ Demonstrated ability to work with multi-discipline, multi-technology teams to drive delivery of research and market access plans
+ Ability to build relationships across the organization and work with different cultures
+ Highly capable to manage complex projects, be strategic and have excellent planning and execution skills
Stryker is a global leader in medical technologies and, together with its customers, is driven to make healthcare better. The company offers innovative products and services in MedSurg, Neurotechnology, Orthopaedics and Spine that help improve patient and healthcare outcomes. Alongside its customers around the world, Stryker impacts more than 150 million patients annually.
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
This advertiser has chosen not to accept applicants from your region.
8
Staff Research Scientist, Machine Learning Efficiency
Sydney, New South Wales
Google
Posted 8 days ago
Job Viewed
Job Description
At Google, we have a vision of empowerment and equitable opportunity for all Aboriginal and Torres Strait Islander peoples and commit to building reconciliation through Google's technology, platforms and people and we welcome Indigenous applicants. Please see our Reconciliation Action Plan ( for more information.
Minimum qualifications:
+ PhD in Computer Science, a related technical field, or equivalent practical experience.
+ 4 years of experience with research agendas across multiple teams or projects in Machine Learning (ML) efficiency, optimization, or a related field.
+ Experience with programming languages (e.g., Python, C or C++).
+ Experience implementing, running, analyzing experimental models or transformer architecture.
+ One or more scientific publication submissions for conferences, journals, or public repositories (e.g., ICML, ICLR, NeurIPS).
Preferred qualifications:
+ Experience in innovative research.
+ Experience as a leader within a research team.
+ Knowledge of existing hardware capabilities and constraints.
+ Understanding of chip design.
+ Ability to navigate ambiguity.
As an organization, Google maintains a portfolio of research projects driven by fundamental research, new product innovation, product contribution and infrastructure goals, while providing individuals and teams the freedom to emphasize specific types of work. As a Research Scientist, you'll setup large-scale tests and deploy promising ideas quickly and broadly, managing deadlines and deliverables while applying the latest theories to develop new and improved products, processes, or technologies. From creating experiments and prototyping implementations to designing new architectures, our research scientists work on real-world problems that span the breadth of computer science, such as machine (and deep) learning, data mining, natural language processing, hardware and software performance analysis, improving compilers for mobile platforms, as well as core search and much more.
As a Research Scientist, you'll also actively contribute to the wider research community by sharing and publishing your findings, with ideas inspired by internal projects as well as from collaborations with research programs at partner universities and technical institutes all over the world.
In this role, you will lead our Machine Learning (ML) efficiency effort. You will work on next-generation large language models architecture, in partnership with hardware engineers and researchers. You will co-design high-performance models along with the next generation of ML accelerators (TPUs) that can power them.
Google Research is building the next generation of intelligent systems for all Google products. To achieve this, we're working on projects that utilize the latest computer science techniques developed by skilled software developers and research scientists. Google Research teams collaborate closely with other teams across Google, maintaining the flexibility and versatility required to adapt new projects and foci that meet the demands of the world's fast-paced business needs.
+ Generate, design ideas, leading a team for finding solutions through theoretical or empirical insights.
+ Design and implementing Machine Learning (ML) algorithms, running and analyzing experiments, incorporating components that could constitute part of a future Tensor Processing Unit (TPU).
+ Collaborate with research teams located across the globe.
+ Define long-term research agendas, intermediate milestones, and align with research and product partners.
+ Impact through publication and scientific dissemination.
Google is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. See also and If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form:
Minimum qualifications:
+ PhD in Computer Science, a related technical field, or equivalent practical experience.
+ 4 years of experience with research agendas across multiple teams or projects in Machine Learning (ML) efficiency, optimization, or a related field.
+ Experience with programming languages (e.g., Python, C or C++).
+ Experience implementing, running, analyzing experimental models or transformer architecture.
+ One or more scientific publication submissions for conferences, journals, or public repositories (e.g., ICML, ICLR, NeurIPS).
Preferred qualifications:
+ Experience in innovative research.
+ Experience as a leader within a research team.
+ Knowledge of existing hardware capabilities and constraints.
+ Understanding of chip design.
+ Ability to navigate ambiguity.
As an organization, Google maintains a portfolio of research projects driven by fundamental research, new product innovation, product contribution and infrastructure goals, while providing individuals and teams the freedom to emphasize specific types of work. As a Research Scientist, you'll setup large-scale tests and deploy promising ideas quickly and broadly, managing deadlines and deliverables while applying the latest theories to develop new and improved products, processes, or technologies. From creating experiments and prototyping implementations to designing new architectures, our research scientists work on real-world problems that span the breadth of computer science, such as machine (and deep) learning, data mining, natural language processing, hardware and software performance analysis, improving compilers for mobile platforms, as well as core search and much more.
As a Research Scientist, you'll also actively contribute to the wider research community by sharing and publishing your findings, with ideas inspired by internal projects as well as from collaborations with research programs at partner universities and technical institutes all over the world.
In this role, you will lead our Machine Learning (ML) efficiency effort. You will work on next-generation large language models architecture, in partnership with hardware engineers and researchers. You will co-design high-performance models along with the next generation of ML accelerators (TPUs) that can power them.
Google Research is building the next generation of intelligent systems for all Google products. To achieve this, we're working on projects that utilize the latest computer science techniques developed by skilled software developers and research scientists. Google Research teams collaborate closely with other teams across Google, maintaining the flexibility and versatility required to adapt new projects and foci that meet the demands of the world's fast-paced business needs.
+ Generate, design ideas, leading a team for finding solutions through theoretical or empirical insights.
+ Design and implementing Machine Learning (ML) algorithms, running and analyzing experiments, incorporating components that could constitute part of a future Tensor Processing Unit (TPU).
+ Collaborate with research teams located across the globe.
+ Define long-term research agendas, intermediate milestones, and align with research and product partners.
+ Impact through publication and scientific dissemination.
Google is proud to be an equal opportunity workplace and is an affirmative action employer. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. We also consider qualified applicants regardless of criminal histories, consistent with legal requirements. See also and If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form:
This advertiser has chosen not to accept applicants from your region.
9