15 Research Roles jobs in Australia

Research fellow and soil

4111 Nathan, Queensland Griffith University

Posted 25 days ago

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Job Description

full time

Every institution values excellence. What matters most is why.

Griffith was created to be a different type of university. You’ll find we’re about leading research, academic excellence, and the transformative power of education. But what sets us apart is why those things matter and how you’ll achieve them.


Why? Griffith brings together exceptional minds like yours from across the globe and from all walks of life. Here, we do incredible work, questioning and challenging, always in the pursuit of excellence.


Job Description

The School of Environment and Science maintains an illustrious research position across numerous industry sectors, guiding and informing its learning and teaching. Our school is committed to contributing to the planet's sustainable future by identifying and measuring environmental problems and offering solution-driven approaches. Our research and teaching staff are acknowledged as world industry leaders, working across the broad science and environment disciplines enabling us to develop and deliver comprehensive study programs. We partner with industry, government, and the community to drive innovation and achieve success.


We are seeking a highly motivated Research Fellow to join our interdisciplinary team (integrated soil science, computational modelling and hyperspectral imaging) at the School of Environment and Science and the Australian Rivers Institute.


The Research Fellow will undertake research in the areas of dynamics of soil carbon and biogeochemistry using cutting-edge hyperspectral imaging, machine learning and modelling techniques. This position offers the opportunity to work at the forefront of soil science and data analytics, aiming to improve our understanding of soil carbon processes, their spatial and temporal variability, and long-term carbon sequestration. The successful candidate will contribute to both research excellence and teaching innovation in environmental and soil sciences.


The Research Fellow position will have a combined academic profile of 60% research, 30% teaching within the School in the fields of soil and earth sciences and 10% Service.


In addition to the above, the position will:


  • Develop and apply machine learning models to extract meaningful patterns from spectral datasets and predict key soil biogeochemical properties.
  • Integrate spectral data with laboratory analyses to understand mechanisms of soil carbon storage and stabilization.
  • Build and maintain spectral libraries of soil samples across different land uses, soil types, and climate zones to support broader modelling and scaling efforts.
  • Publish high-quality research outputs in peer-reviewed journals, contribute to grant applications and project reports, and present findings at national and international conferences.
  • Supervise and mentor research students and assistants, while contributing to undergraduate and postgraduate teaching in Soil Science and Earth Science to enhance student engagement and learning outcomes.
  • Collaborate across disciplines and engage with external stakeholders to co-develop research methodologies, support research group activities, and strengthen the School’s research profile and community impact.


This is a fixed term (12 months), full time position primarily based at Griffith University Brisbane South (Nathan). As Griffith is a multi-campus University you may be required to work across other campus locations.


Griffith University’s sites are located on the lands of the Yugarabul, Yuggera, Jagera, Turrbal, Yugambeh and Kombumerri peoples.


Salary Range

The full time equivalent base salary will be Research Fellow Grade 2 range $113,226 - $34,460 per annum + 17% superannuation. The total FTE package will be in the range 132,474 - 157,318 per annum.


Qualifications

The successful candidate for this position will hold a PhD in Soil Science, Computer Science, Environmental Science, Geoinformatics, Machine learning, or a related field.


You will also have:


  • Experience with hyperspectral or spectroscopic or computational analysis of soils or natural materials.
  • Proficiency in machine learning (e.g., Python, R, MATLAB) and multivariate data analysis.
  • A strong track record of publishing high-quality research in peer-reviewed, high-impact journals, with experience presenting findings at national and international conferences.
  • Demonstrated ability to work independently and collaboratively within interdisciplinary research teams, managing competing deadlines while maintaining effective communication with diverse stakeholders.
  • Experience delivering engaging lectures and tutorials in the fields of soil and earth sciences.


Additional Information


Why Griffith?

As a values-led organisation, at Griffith University, we've worked hard to create a dynamic and strong organisational culture. We offer:


  • Mix of on campus and work from home options available and a supportive work environment
  • Generous leave entitlements including paid parental leave and leave loading
  • Health Safety and Wellbeing initiatives – on campus Gym facilities


How to apply

At Griffith, we’re committed to providing a safe and inclusive environment for all - whoever you are and wherever you’re from. If you require any accommodations, we welcome you to let us know so we can work with you to participate fully in our recruitment experience.


Griffith University values diversity, inclusion and flexibility and we encourage Aboriginal and Torres Strait Islander, and people of all backgrounds to apply. For more information please visit our Equity, Diversity and Inclusion page. Griffith University also maintains a strict zero-tolerance policy against all forms of modern slavery. For more information, please refer to Griffith’s Modern Slavery Policy.


Please submit your application online and ensure it includes the following:


  • A covering letter outlining your suitability for the role (please refer to the qualifications above and the position description)
  • Current curriculum vitae/resume including full contact details
  • Names and contact details of at least three professional referees (no contact will be made without your permission)


Applicants must have unrestricted working rights. VISA sponsorship is not available for this position.


For further information specifically about this role, please contact Distinguished Professor Chengrong Chen, School of Environment and Science at


For application and recruitment advice, please contact Ms Corinna Gartrell, Talent Acquisition Partner at


For application support, please contact People Services on +61 7 373 54011 and quote reference number REF8182F.


Closing date: Wednesday 30 July 2025 at 11:59pm AEST. All applications must be submitted online.

This advertiser has chosen not to accept applicants from your region.

Site Research Assistant - Condord

North Sydney, New South Wales IQVIA

Posted 10 days ago

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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 advertiser has chosen not to accept applicants from your region.

Research Assistant Volunteer (Global/Remote) - Help Change the Wo

Brisbane, Queensland UniversalGiving(R)

Posted 12 days ago

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Job Summary
Volunteers: Volunteers have a heart for giving back. The Research Assistant works on important, diverse research projects as needed by the Operations Team. We are excited to have you join our global team and help serve the world in philanthropy. br>
About us
UniversalGiving® is an award-winning nonprofit allowing people to donate and volunteer with top-performing, vetted organizations all over the world. 100% goes directly to the cause. All partner organizations are vetted with our proprietary Quality Model®. UniversalGiving® has been featured on the homepage of Bloomberg, Oprah.com, CBS, The Wall Street Journal, and The New York Times. UniversalGiving® also has been featured in more than 16 books, including the new edition Harvard Business Review Book, HBR Guide to Delivering Effective Feedback, Arianna Huffington’s Thrive, and Laura Arrillaga-Andreessen’s Giving 2.0. We have also been acknowledged six times on Great Nonprofits’ annual Top Nonprofits lists and are highlighted in Huffington Post's list of best volunteering matching websites. We continue to gain momentum, with dozens of articles in the Christian Science Monitor and monthly contributions on Forbes. To date, we have matched more than 22,000 volunteers worth $31 million dollars’ of volunteer hours.

Re ponsibilities:
- Research high-net-worth potential and existing donors, foundations, and corporations
- Research journalists, universities, and celebrities to develop marketing partnerships
- Research Tech for Good companies
- Research Tools across Marketing, Operations, Product Development
- Record, update, and manage data in spreadsheets and Salesforce
- With proven success & a positive attitude, take on special projects and new responsibilities

Qualifications
- Excellent written and verbal communication skills
- Meticulous attention to detail
- Ability to thrive in a fast-paced environment
- Competence with Salesforce and Google Drive
- Willingness to learn new technologies

Benefits
- Part-time, flexible, remote positions
- Opportunity to work with a diverse, global team representing over 25 cultures
- Gain experience with a Tech for Good nonprofit
- With proven success & a positive attitude, UniversalGiving® is likely to facilitate J1, OPT visas br>
Duration and Location
- The position is available part-time (5-20 hours per week)
- Minimum 6 months commitment
- We provide remote positions with a highly globally focused team from more than 20 countries, including Russia, China, Japan, Ukraine, Georgia, the Philippines, Haiti, Germany, Canada, the Kurdish population, South Korea, the U.K., Brazil, and many more
This advertiser has chosen not to accept applicants from your region.

Research Assistant Intern (Global/Remote) - Help Change the World

Canberra, Australian Capital Territory UniversalGiving(R)

Posted 16 days ago

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Job Description

Job Summary
Internship: Internships are for people in school or with a few years of experience. The Research Assistant Intern works on important, diverse research projects as needed by the Operations Team. We are excited to have you join our global team and help serve the world in philanthropy. br>
About us
UniversalGiving® is an award-winning nonprofit allowing people to donate and volunteer with top-performing, vetted organizations all over the world. 100% goes directly to the cause. All partner organizations are vetted with our proprietary Quality Model®. UniversalGiving® has been featured on the homepage of Bloomberg, Oprah.com, CBS, The Wall Street Journal, and The New York Times. UniversalGiving® also has been featured in more than 16 books, including the new edition Harvard Business Review Book, HBR Guide to Delivering Effective Feedback, Arianna Huffington’s Thrive, and Laura Arrillaga-Andreessen’s Giving 2.0. We have also been acknowledged six times on Great Nonprofits’ annual Top Nonprofits lists and are highlighted in Huffington Post's list of best volunteering matching websites. We continue to gain momentum, with dozens of articles in the Christian Science Monitor and monthly contributions on Forbes. To date, we have matched more than 22,000 volunteers worth $31 million dollars’ of volunteer hours.

Re ponsibilities
- Perform research on high net-worth potential and existing donors, foundations, and corporations
- Research on journalists, universities, and celebrities to develop marketing partnerships
- Perform research on Tech for Good companies
- Filling out Competitive Matrices for Operations, evaluating pros/cons of services we may use
- Research on Product Development Tools
- Research and update Event Planning Matrices/Tools
- Record all data in Salesforce
- Record and update all spreadsheets

Qualifications
- Excellent written and verbal communication skills
- Meticulous attention to detail
- Ability to thrive in a fast-paced environment
- Competence with Salesforce and Google Drive
- Willingness to learn new technologies

Benefits
- Part-time, flexible, remote positions
- Opportunity to work with a diverse, global team representing over 25 cultures
- Gain experience with a Tech for Good nonprofit
- With proven success & a positive attitude, UniversalGiving® is likely to facilitate J1, OPT visas br>
Duration and Location
- The position is available part-time (5-20 hours per week)
- Minimum 6 months commitment
- We provide remote positions with a highly globally focused team from more than 20 countries, including Russia, China, Japan, Ukraine, Georgia, the Philippines, Haiti, Germany, Canada, the Kurdish population, South Korea, the U.K., Brazil, and many more
This advertiser has chosen not to accept applicants from your region.

Clinical Research Associate 2

North Sydney, New South Wales IQVIA

Posted 10 days ago

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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
This advertiser has chosen not to accept applicants from your region.

Senior Clinical Research Associate

Adelaide, South Australia IQVIA

Posted 10 days ago

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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
This advertiser has chosen not to accept applicants from your region.

Senior Clinical Research Associate

Brisbane, Queensland IQVIA

Posted 10 days ago

Job Viewed

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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
This advertiser has chosen not to accept applicants from your region.
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Senior Clinical Research Associate

Melbourne, Victoria IQVIA

Posted 10 days ago

Job Viewed

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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
This advertiser has chosen not to accept applicants from your region.

Senior Clinical Research Associate

Perth, Western Australia IQVIA

Posted 10 days ago

Job Viewed

Tap Again To Close

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
This advertiser has chosen not to accept applicants from your region.

Senior Clinical Research Associate

North Sydney, New South Wales IQVIA

Posted 10 days ago

Job Viewed

Tap Again To Close

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.
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