What Clinical Research Jobs are in Australia?
Showing 86 Clinical Research jobs in Australia
Job Description
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com ( .
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
**Job Function:**
R&D Operations
**Job Sub** **Function:**
Clinical Trial Project Management
**Job Category:**
People Leader
**All Job Posting Locations:**
North Ryde, New South Wales, Australia
**Job Description:**
DePuy Synthes is recruiting for a Manager, Clinical Research in North Ryde, Australia
+ **Join our change journey at J&J-help shape what's next**
+ **Step into a high-impact career opportunity with real visibility**
**THE OPPORTUNITY**
The Manager, Clinical Research which plays a critical leadership role in the planning, execution, and oversight of clinical research activities supporting DePuy Synthes' orthopedic portfolio. This role partners closely with cross‑functional stakeholders to ensure clinical studies are scientifically sound, operationally efficient, and compliant with global and local regulatory requirements. The position offers the opportunity to directly influence evidence generation that supports patient outcomes, product innovation, and regulatory and commercial success.
**RESPONSIBILITIES**
+ Lead end-to-end clinical study operations across assigned programs, including feasibility planning, vendor/CRO engagement, start-up, execution, and close-out activities.
+ Drive clinical site identification and selection by leading feasibility assessments (site experience, enrollment potential, quality history, contracting/start-up timelines), documenting rationale, and aligning final site lists with study strategy.
+ Ensure studies are executed in compliance with GCP, applicable country regulations, and internal procedures, including oversight of informed consent, safety reporting, essential documents, and data integrity expectations.
+ Serve as a primary clinical operations point of contact to cross-functional stakeholders (R&D, Medical Affairs, Regulatory, Quality, Biostatistics/Data Management) and external partners (CROs, investigators), ensuringtimelydecisions and clear documentation of actions and outcomes.
+ Develop andmaintainoperational study plans (milestones, enrollment projections, monitoring strategy, issue escalation pathways), track progress against timelines and budget, and proactively identify/mitigate risks to deliverables.
+ Own monitoring resourcing planning (FTE/visit forecasts, CRA allocation, coverage models) and coordinate with monitoring leadership/CROs to ensure adequate capacity, continuity, and quality oversight across sites.
+ Support inspection readiness andparticipatein audits/inspections by preparing study documentation, coordinating responses,facilitatinginterviews, and drivingtimelycompletion of corrective and preventive actions (CAPAs) for study-related findings.
+ Drive consistent project management and communication practices, including meeting cadences, status reporting, and lessons learned; collaborate effectively with a US-based global clinical team by planning across time zones and ensuringtimelyhandoffs and stakeholder updates.
**ABOUT YOU**
**Required:**
+ Bachelor's degree in Life Sciences, Health Sciences, Engineering, ora relateddiscipline (required).
+ 6-8 years of progressive experience in clinical research, clinical operations, or related medical device or healthcare research roles.
+ Demonstrated experience managing or leading clinical studies andcross‑functionalteams.
+ Strong knowledge of GCP, clinical research regulations, and quality systems.
+ Proven ability to manage multiple priorities, timelines, and stakeholders in a matrix environment.
+ Excellent written and verbal communication skills, including scientific and clinical documentation.
**Desirable:**
+ Advanced degree (Master'sor PhD) in a scientific or clinical discipline (preferred).
+ Experience within medical devices, orthopedics, or surgical products.
+ Priorpeople‑managementor matrix leadership experience.
+ Experience supporting regulatory submissions orpost‑marketclinical studies.
+ Familiarity with global clinical trial execution andinvestigator‑initiatedresearch.
**Other:**
+ Language: Englishproficiencyrequired.
+ Travel: Up to 20% domestic and international travel may berequired.
+ Certifications: Clinical research or project management certifications (e.g., ACRP, SOCRA, PMP) preferred.
**COMPANY CULTURE**
+ Competitive remuneration package.
+ Continuous training and support.
+ Award-winning leadership development programs.
+ Inclusive, flexible, and accessible working arrangements.
+ Equal opportunity employer supporting diversity and inclusion.
**WHY CHOOSE US:**
+ Competitive remuneration package and continuous training.
+ Supportive environment with award-winning leadership development programs.
+ Inclusive, flexible, and accessible working arrangements for all.
Johnson & Johnson has announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company. The planned separation is anticipated to be completed within 18 to 24 months, subject to satisfaction of legal and regulatory requirements, and other customary conditions and approvals. Should you accept this position, it is anticipated that following conclusion of the transaction, you would be an employee of the standalone orthopaedics company and your employment would be governed by the standalone orthopaedics company's employment processes, programs, policies and benefit plans. In that case, details of any planned changes would be provided to you by the standalone orthopaedics company at an appropriate time and subject to any necessary consultation processes.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via ( , internal employees contact AskGS to be directed to your accommodation resource.
\#LI-Hybrid
\#DePuySynthesCareers
**Required Skills:**
**Preferred Skills:**
Budgeting, Clinical Trial Management Systems (CTMS), Clinical Trials, Compliance Management, Contract Management, Developing Others, Execution Focus, Fact-Based Decision Making, Inclusive Leadership, Laboratory Operations, Leadership, Process Improvements, Program Management, Project Integration Management, Research and Development, Research Ethics, Resource Planning, Team Management
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
**Job Function:**
R&D Operations
**Job Sub** **Function:**
Clinical Trial Project Management
**Job Category:**
People Leader
**All Job Posting Locations:**
North Ryde, New South Wales, Australia
**Job Description:**
DePuy Synthes is recruiting for a Manager, Clinical Research in North Ryde, Australia
+ **Join our change journey at J&J-help shape what's next**
+ **Step into a high-impact career opportunity with real visibility**
**THE OPPORTUNITY**
The Manager, Clinical Research which plays a critical leadership role in the planning, execution, and oversight of clinical research activities supporting DePuy Synthes' orthopedic portfolio. This role partners closely with cross‑functional stakeholders to ensure clinical studies are scientifically sound, operationally efficient, and compliant with global and local regulatory requirements. The position offers the opportunity to directly influence evidence generation that supports patient outcomes, product innovation, and regulatory and commercial success.
**RESPONSIBILITIES**
+ Lead end-to-end clinical study operations across assigned programs, including feasibility planning, vendor/CRO engagement, start-up, execution, and close-out activities.
+ Drive clinical site identification and selection by leading feasibility assessments (site experience, enrollment potential, quality history, contracting/start-up timelines), documenting rationale, and aligning final site lists with study strategy.
+ Ensure studies are executed in compliance with GCP, applicable country regulations, and internal procedures, including oversight of informed consent, safety reporting, essential documents, and data integrity expectations.
+ Serve as a primary clinical operations point of contact to cross-functional stakeholders (R&D, Medical Affairs, Regulatory, Quality, Biostatistics/Data Management) and external partners (CROs, investigators), ensuringtimelydecisions and clear documentation of actions and outcomes.
+ Develop andmaintainoperational study plans (milestones, enrollment projections, monitoring strategy, issue escalation pathways), track progress against timelines and budget, and proactively identify/mitigate risks to deliverables.
+ Own monitoring resourcing planning (FTE/visit forecasts, CRA allocation, coverage models) and coordinate with monitoring leadership/CROs to ensure adequate capacity, continuity, and quality oversight across sites.
+ Support inspection readiness andparticipatein audits/inspections by preparing study documentation, coordinating responses,facilitatinginterviews, and drivingtimelycompletion of corrective and preventive actions (CAPAs) for study-related findings.
+ Drive consistent project management and communication practices, including meeting cadences, status reporting, and lessons learned; collaborate effectively with a US-based global clinical team by planning across time zones and ensuringtimelyhandoffs and stakeholder updates.
**ABOUT YOU**
**Required:**
+ Bachelor's degree in Life Sciences, Health Sciences, Engineering, ora relateddiscipline (required).
+ 6-8 years of progressive experience in clinical research, clinical operations, or related medical device or healthcare research roles.
+ Demonstrated experience managing or leading clinical studies andcross‑functionalteams.
+ Strong knowledge of GCP, clinical research regulations, and quality systems.
+ Proven ability to manage multiple priorities, timelines, and stakeholders in a matrix environment.
+ Excellent written and verbal communication skills, including scientific and clinical documentation.
**Desirable:**
+ Advanced degree (Master'sor PhD) in a scientific or clinical discipline (preferred).
+ Experience within medical devices, orthopedics, or surgical products.
+ Priorpeople‑managementor matrix leadership experience.
+ Experience supporting regulatory submissions orpost‑marketclinical studies.
+ Familiarity with global clinical trial execution andinvestigator‑initiatedresearch.
**Other:**
+ Language: Englishproficiencyrequired.
+ Travel: Up to 20% domestic and international travel may berequired.
+ Certifications: Clinical research or project management certifications (e.g., ACRP, SOCRA, PMP) preferred.
**COMPANY CULTURE**
+ Competitive remuneration package.
+ Continuous training and support.
+ Award-winning leadership development programs.
+ Inclusive, flexible, and accessible working arrangements.
+ Equal opportunity employer supporting diversity and inclusion.
**WHY CHOOSE US:**
+ Competitive remuneration package and continuous training.
+ Supportive environment with award-winning leadership development programs.
+ Inclusive, flexible, and accessible working arrangements for all.
Johnson & Johnson has announced plans to separate our Orthopaedics business to establish a standalone orthopaedics company. The planned separation is anticipated to be completed within 18 to 24 months, subject to satisfaction of legal and regulatory requirements, and other customary conditions and approvals. Should you accept this position, it is anticipated that following conclusion of the transaction, you would be an employee of the standalone orthopaedics company and your employment would be governed by the standalone orthopaedics company's employment processes, programs, policies and benefit plans. In that case, details of any planned changes would be provided to you by the standalone orthopaedics company at an appropriate time and subject to any necessary consultation processes.
Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.
Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants' needs. If you are an individual with a disability and would like to request an accommodation, external applicants please contact us via ( , internal employees contact AskGS to be directed to your accommodation resource.
\#LI-Hybrid
\#DePuySynthesCareers
**Required Skills:**
**Preferred Skills:**
Budgeting, Clinical Trial Management Systems (CTMS), Clinical Trials, Compliance Management, Contract Management, Developing Others, Execution Focus, Fact-Based Decision Making, Inclusive Leadership, Laboratory Operations, Leadership, Process Improvements, Program Management, Project Integration Management, Research and Development, Research Ethics, Resource Planning, Team Management
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Apply Now
0
Job Description
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You'll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
**A Day in the Life**
This is an excellent opportunity to join a leading global medical technology, with a mission to contribute to human welfare by application of biomedical engineering in the research, design, manufacture, and sale of instruments or appliances that **alleviate pain** , **restore health** , and **extend life** .
The Senior Clinical Research Manager leads a high‑performing team overseeing end‑to‑end clinical research operations across ANZ. The role partners closely with regional and global operating units, as well as cross‑functional teams, to deliver clinical research programs from inception through completion.
**Responsibilities may include the following and other duties may be assigned:**
**CLINICAL STRATEGY AND EXECUTION**
+ Strategic partner for the ANZ Commercial Operating Unit (OU) Leaders and spearheading the development of Clinical Research and Medical Science (CRMS) in ANZ aligned to the needs of the region.
+ Provides input to the local clinical strategy and ensures full alignment with the global clinical strategy.
+ Identifies potential local/regional clinical studies in line with local/regional and OU strategy
+ Partners & collaborates with global CRMS OU Leaders to position ANZ as the place to go for pre/post market studies
+ Develops and implements strategies to support regulatory function to obtain timely product approvals from regional regulatory bodies.
+ Represents Medtronic from clinical research respective within the country / region and collects insights from local customers and authorities.
+ Builds and maintains a strong network and close relationship with the various internal and external stakeholders.
+ Leads execution for both local and global studies, manages clinical research projects over all of the Medtronic therapies across multiple businesses.
+ Ensures appropriate resources and priorities are maintained for the projects assigned to the geography/country.
+ Develop clinical project/study and documents in collaboration with relevant stakeholders within Medtronic and oversee the execution in region.
+ Assures successful & timely execution of assigned clinical programs consistent with clinical plans and applicable regulations and policies interfacing with representatives from key functional groups within Medtronic.
+ Develops and manages the study- and cost centre budgets.
+ Advises local marketing organization on outcome of publications and advises on a communication strategy.
**PEOPLE MANAGEMENT**
+ Leads and manages a team of clinical professionals and related staffs including Management and supervisory professionals.
+ Manages cross functional teams and stakeholders in accordance with the tasks linked to local or global clinical projects.
+ Manages hiring, objective setting and appraisals mainly focusing on aligning projects (objectives, strategy, scope, and schedule) according to and to meet business plans.
+ Provide leadership to staff ensuring the prioritization of strategic and department level initiatives to include defining performance goals and targets, conducting performance reviews, and staff 1:1s to guide performance management and employee development efforts and manage toward departmental goals.
**EXTERNAL RELATIONS**
+ Builds and maintains a strong network with key-opinion leaders and relevant external stakeholders (Scientific Societies, Regulators, Advisory Groups etc.) specific to the country/region.
+ Ensures intake for investigator-initiated research ideas and ensure appropriate follow-up within the organization through the relevant policy and SOP.
+ Be the first point of contact for:
+ Local customers, authorities and KOLs about local Clinical Affairs
+ Builds the right level of knowledge in reimbursement, health management in the country/region to address those with relevant clinical solutions.
**Required Knowledge and Experience:**
+ Requires a Master's Degree in relevant Science or biomedical field (Medicine, Biomedical Engineering, Medical Physics, Medical Biology, Health Sciences, etc.) and a minimum of 10 years of experience in clinical research and operation with 5+ years of managerial experience.
+ Requires broad management knowledge to lead project teams in one department.
+ Typically has mastery level knowledge and skills within a specific technical or professional discipline with broad understanding of other areas within the job function.
+ Demonstrable experience in First in Human, Pre-market and post market clinical study planning and execution.
+ Strong knowledge of local legal and regulatory requirements for conduct of clinical trial
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email
**A Day in the Life**
This is an excellent opportunity to join a leading global medical technology, with a mission to contribute to human welfare by application of biomedical engineering in the research, design, manufacture, and sale of instruments or appliances that **alleviate pain** , **restore health** , and **extend life** .
The Senior Clinical Research Manager leads a high‑performing team overseeing end‑to‑end clinical research operations across ANZ. The role partners closely with regional and global operating units, as well as cross‑functional teams, to deliver clinical research programs from inception through completion.
**Responsibilities may include the following and other duties may be assigned:**
**CLINICAL STRATEGY AND EXECUTION**
+ Strategic partner for the ANZ Commercial Operating Unit (OU) Leaders and spearheading the development of Clinical Research and Medical Science (CRMS) in ANZ aligned to the needs of the region.
+ Provides input to the local clinical strategy and ensures full alignment with the global clinical strategy.
+ Identifies potential local/regional clinical studies in line with local/regional and OU strategy
+ Partners & collaborates with global CRMS OU Leaders to position ANZ as the place to go for pre/post market studies
+ Develops and implements strategies to support regulatory function to obtain timely product approvals from regional regulatory bodies.
+ Represents Medtronic from clinical research respective within the country / region and collects insights from local customers and authorities.
+ Builds and maintains a strong network and close relationship with the various internal and external stakeholders.
+ Leads execution for both local and global studies, manages clinical research projects over all of the Medtronic therapies across multiple businesses.
+ Ensures appropriate resources and priorities are maintained for the projects assigned to the geography/country.
+ Develop clinical project/study and documents in collaboration with relevant stakeholders within Medtronic and oversee the execution in region.
+ Assures successful & timely execution of assigned clinical programs consistent with clinical plans and applicable regulations and policies interfacing with representatives from key functional groups within Medtronic.
+ Develops and manages the study- and cost centre budgets.
+ Advises local marketing organization on outcome of publications and advises on a communication strategy.
**PEOPLE MANAGEMENT**
+ Leads and manages a team of clinical professionals and related staffs including Management and supervisory professionals.
+ Manages cross functional teams and stakeholders in accordance with the tasks linked to local or global clinical projects.
+ Manages hiring, objective setting and appraisals mainly focusing on aligning projects (objectives, strategy, scope, and schedule) according to and to meet business plans.
+ Provide leadership to staff ensuring the prioritization of strategic and department level initiatives to include defining performance goals and targets, conducting performance reviews, and staff 1:1s to guide performance management and employee development efforts and manage toward departmental goals.
**EXTERNAL RELATIONS**
+ Builds and maintains a strong network with key-opinion leaders and relevant external stakeholders (Scientific Societies, Regulators, Advisory Groups etc.) specific to the country/region.
+ Ensures intake for investigator-initiated research ideas and ensure appropriate follow-up within the organization through the relevant policy and SOP.
+ Be the first point of contact for:
+ Local customers, authorities and KOLs about local Clinical Affairs
+ Builds the right level of knowledge in reimbursement, health management in the country/region to address those with relevant clinical solutions.
**Required Knowledge and Experience:**
+ Requires a Master's Degree in relevant Science or biomedical field (Medicine, Biomedical Engineering, Medical Physics, Medical Biology, Health Sciences, etc.) and a minimum of 10 years of experience in clinical research and operation with 5+ years of managerial experience.
+ Requires broad management knowledge to lead project teams in one department.
+ Typically has mastery level knowledge and skills within a specific technical or professional discipline with broad understanding of other areas within the job function.
+ Demonstrable experience in First in Human, Pre-market and post market clinical study planning and execution.
+ Strong knowledge of local legal and regulatory requirements for conduct of clinical trial
**Physical Job Requirements**
The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
**Benefits & Compensation**
**Medtronic offers a competitive Salary and flexible Benefits Package**
A commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.
This position is eligible for a short-term incentive called the Medtronic Incentive Plan (MIP).
**About Medtronic**
We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
Learn more about our business, mission, and our commitment to diversity here ( lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.
Our Mission - to alleviate pain, restore health, and extend life - unites a global team of 95,000+ passionate people.
We are engineers at heart- putting ambitious ideas to work to generate real solutions for real people. From the R&D lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary.
**We change lives** . Each team member, each day, helps to improve and redefine how the world treats the most pressing health conditions, from heart disease to diabetes. Our industry leadership comes from the passion and ingenuity of our people. That's who we are. Working alongside one another, we use science, medicine, and a profound understanding of the human body to build extraordinary technologies that can transform lives.
**We build extraordinary solutions as one team** . With one Medtronic Mindset defining how we work. Speed and decisiveness run through our DNA. Diverse perspectives inspire our bold answers to any challenge that comes our way. And we deliver results the right way, breakthrough after patient breakthrough.
**This life-changing career is yours to engineer** . By bringing your ambitious ideas, unique perspective and contributions, you will.
+ **Build** a better future, amplifying your impact on the causes that matter to you and the world
+ **Grow** a career reflective of your passion and abilities
+ **Connect** to a dynamic and inclusive culture that welcomes the challenge of life-long learning
These commitments set our team apart from the rest:
**Experiences that put people first** . Respect for people is the hallmark of our humanity. It fuels our team to positively impact even a single life. And it means we put our people first at Medtronic as well, creating a culture of belonging and always pushing to get you the career-building resources you need.
**Life-transforming technologies** . No matter your role, you contribute to technologies that transform lives. What we build empowers patients to live life on their terms.
**Better outcomes for our world** . Here, it's about more than the bottom line. Our Mission to improve human welfare drives us. We advance healthcare, society, and equity with every design, inside and outside our walls.
**Insight-driven care** . Fresh viewpoints. Cutting-edge AI, data, and automation. You're shaping the future of healthcare technology and defining the next generation of breakthroughs in care
It is the policy of Medtronic to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by federal, state or local law. In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities.
For sales reps and other patient facing field employees, going into a healthcare setting is considered an essential function of the job and we expect our employees to comply with all credentialing requirements at the hospitals or clinics they support.
This employer participates in the federal E-Verify program to confirm the identity and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here ( .
For updates on job applications, please go to the candidate login page and sign in to check your application status.
If you need assistance completing your application please email
To request removal of your personal information from our systems please email
Is this job a match or a miss?
Apply Now
1
Experienced CRCs & CRAs | Relocate to Brisbane and Advance Your Clinical Research Career
Brisbane
ThermoFisher Scientific
Posted 4 days ago
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
**Australia and New Zealand Candidates are welcome to apply**
**Relocation support to Brisbane may be provided for the successful candidate**
**Location:** Brisbane, Australia (Home-based, 100% Remote)
**Employment Type:** Full-time
At PPD, part of Thermo Fisher Scientific, you'll be part of a global team helping bring innovative, life-changing treatments to patients faster. We partner with leading pharmaceutical and biotechnology companies to advance groundbreaking therapies across a wide range of therapeutic areas. In addition to making a meaningful impact on patients' lives, you'll have access to exceptional opportunities for career growth, professional development, and global collaboration within one of the world's leading healthcare and life sciences organizations. Join us and build a career where your work matters, your development is supported, and your contributions help shape the future of healthcare.
**Why Join Us?**
+ Opportunity to **build your career while establishing yourself in Brisbane** , one of Australia's fastest-growing life sciences hubs
+ Structured CRA onboarding and training program tailored to your experience level through our CRA Compass program
+ Dedicated mentorship and clear progression pathway to independent CRA
+ Exposure to a broad range of clinical trials across multiple therapeutic areas and sponsors
+ Competitive salary package, including car/travel allowance and benefits
+ Supportive, collaborative, and growth-focused team culture
**About the Role**
We're looking to connect with clinical research professionals across a range of experience levels-from Study/Clinical Research Coordinators with 5+ years of experience through to CRA I, CRA II, and Senior CRAs-who are based in Australia or New Zealand and are either relocating or genuinely planning to relocate to Brisbane.
Joining our team means becoming part of a collaborative and supportive environment where you'll work on a variety of clinical studies and continue building your expertise. For Coordinators, it's a great opportunity to make the transition into monitoring with the support and development needed to succeed. For experienced CRAs, it's a chance to broaden your experience, take on new challenges, and further develop your career within a global organization dedicated to advancing innovative therapies for patients.
We're particularly interested in candidates who are excited about building their future in Brisbane. For the successful candidate, relocation assistance may be available to help support the move, depending on individual circumstances and business requirements.
**Key Responsibilities**
+ Perform and coordinate all aspects of clinical monitoring and site management, including:
+ Source Data Review (SDR) and Source Data Verification (SDV)
+ Preparation of visit reports
+ Maintenance of accurate and compliant study documentation
+ Identification and resolution of site issues and action items
+ Conduct on-site and remote monitoring visits to ensure protocol and regulatory compliance
+ Ensure studies are conducted in accordance with ICH-GCP, regulatory requirements, and SOPs, safeguarding subject safety and data integrity
+ Maintain audit readiness at all times
+ Build strong, collaborative relationships with investigational sites
+ Partner cross-functionally with Clinical Trial Managers, Study Start-Up, and Regulatory teams
**What We're Looking For**
+ Currently based in Australia or New Zealand, with confirmed plans or readiness to relocate to Brisbane
+ Minimum 5+ years' experience as a Clinical Study/Research Coordinator (sponsor-driven trials), or 6-12 months' experience as a CRA
+ Bachelor's degree in life sciences, nursing, or related field
+ Solid understanding of clinical trials and ICH-GCP guidelines
+ Ability and willingness to travel extensively (70-80%)
+ Valid Australian/New Zealand driver's license
+ Australian or New Zealand citizen, or Australian permanent resident
If you're ready to take the next step in your CRA journey and are **prepared to make Brisbane your base** , we'd love to hear from you.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
**Australia and New Zealand Candidates are welcome to apply**
**Relocation support to Brisbane may be provided for the successful candidate**
**Location:** Brisbane, Australia (Home-based, 100% Remote)
**Employment Type:** Full-time
At PPD, part of Thermo Fisher Scientific, you'll be part of a global team helping bring innovative, life-changing treatments to patients faster. We partner with leading pharmaceutical and biotechnology companies to advance groundbreaking therapies across a wide range of therapeutic areas. In addition to making a meaningful impact on patients' lives, you'll have access to exceptional opportunities for career growth, professional development, and global collaboration within one of the world's leading healthcare and life sciences organizations. Join us and build a career where your work matters, your development is supported, and your contributions help shape the future of healthcare.
**Why Join Us?**
+ Opportunity to **build your career while establishing yourself in Brisbane** , one of Australia's fastest-growing life sciences hubs
+ Structured CRA onboarding and training program tailored to your experience level through our CRA Compass program
+ Dedicated mentorship and clear progression pathway to independent CRA
+ Exposure to a broad range of clinical trials across multiple therapeutic areas and sponsors
+ Competitive salary package, including car/travel allowance and benefits
+ Supportive, collaborative, and growth-focused team culture
**About the Role**
We're looking to connect with clinical research professionals across a range of experience levels-from Study/Clinical Research Coordinators with 5+ years of experience through to CRA I, CRA II, and Senior CRAs-who are based in Australia or New Zealand and are either relocating or genuinely planning to relocate to Brisbane.
Joining our team means becoming part of a collaborative and supportive environment where you'll work on a variety of clinical studies and continue building your expertise. For Coordinators, it's a great opportunity to make the transition into monitoring with the support and development needed to succeed. For experienced CRAs, it's a chance to broaden your experience, take on new challenges, and further develop your career within a global organization dedicated to advancing innovative therapies for patients.
We're particularly interested in candidates who are excited about building their future in Brisbane. For the successful candidate, relocation assistance may be available to help support the move, depending on individual circumstances and business requirements.
**Key Responsibilities**
+ Perform and coordinate all aspects of clinical monitoring and site management, including:
+ Source Data Review (SDR) and Source Data Verification (SDV)
+ Preparation of visit reports
+ Maintenance of accurate and compliant study documentation
+ Identification and resolution of site issues and action items
+ Conduct on-site and remote monitoring visits to ensure protocol and regulatory compliance
+ Ensure studies are conducted in accordance with ICH-GCP, regulatory requirements, and SOPs, safeguarding subject safety and data integrity
+ Maintain audit readiness at all times
+ Build strong, collaborative relationships with investigational sites
+ Partner cross-functionally with Clinical Trial Managers, Study Start-Up, and Regulatory teams
**What We're Looking For**
+ Currently based in Australia or New Zealand, with confirmed plans or readiness to relocate to Brisbane
+ Minimum 5+ years' experience as a Clinical Study/Research Coordinator (sponsor-driven trials), or 6-12 months' experience as a CRA
+ Bachelor's degree in life sciences, nursing, or related field
+ Solid understanding of clinical trials and ICH-GCP guidelines
+ Ability and willingness to travel extensively (70-80%)
+ Valid Australian/New Zealand driver's license
+ Australian or New Zealand citizen, or Australian permanent resident
If you're ready to take the next step in your CRA journey and are **prepared to make Brisbane your base** , we'd love to hear from you.
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
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2
Job Description
**Job Description Summary**
At GE HealthCare, we are enabling precision care through innovative medical technologies, advanced imaging solutions and clinical intelligence.
We are seeking an experienced CT Clinical Insights Specialist to provide strategic clinical leadership across Australia and New Zealand. This highly influential role partners with customers, Key Opinion Leaders (KOLs), commercial teams and product specialists to drive clinical excellence, workflow optimisation and customer success across our Computed Tomography (CT) portfolio.
As a recognised CT expert, you will help shape clinical best practice, support commercial growth, advance customer adoption of innovative technologies and strengthen GE HealthCare's position as a trusted partner in diagnostic imaging.
**Job Description**
**About the Role**
The CT Clinical Insights Specialist role blends clinical expertise, customer engagement and commercial collaboration to deliver exceptional outcomes for healthcare providers throughout the ANZ region.
You will work closely with customers to optimise clinical protocols, improve workflow efficiency and support the adoption of advanced CT technologies. Additionally, you will play a key role in developing KOL relationships, supporting strategic projects and providing advanced clinical education to both customers and internal teams.
**Key Responsibilities**
**Clinical Leadership & Commercial Support**
+ Provide high-level clinical expertise during customer engagements, demonstrations and site visits.
+ Support strategic sales opportunities, large capital projects and tender submissions.
+ Demonstrate the clinical and operational value of GE HealthCare CT solutions.
+ Collaborate closely with Sales, Marketing, Service and Leadership teams to support business objectives and customer outcomes.
**Customer Success & Clinical Optimisation**
+ Partner with healthcare providers to optimise CT clinical protocols and workflow efficiency.
+ Identify opportunities to enhance clinical performance and improve operational outcomes.
+ Act as a trusted advisor to radiology leaders, clinicians and imaging departments.
+ Stay connected to evolving customer needs and emerging healthcare challenges.
**Key Opinion Leader & Market Development**
+ Develop and maintain relationships with leading CT clinicians and industry influencers across ANZ.
+ Support the development and ongoing success of reference and showcase sites.
+ Collaborate with KOLs on the evaluation of new techniques, clinical advancements and research initiatives.
+ Build relationships with academic institutions, professional societies and healthcare stakeholders.
+ Contribute to marketing initiatives and support execution of regional growth strategies.
**Education & Clinical Excellence**
+ Deliver advanced customer training and education programs.
+ Support the professional development of internal commercial and clinical teams.
+ Promote clinical differentiation and evidence-based value propositions across the CT portfolio.
+ Maintain expert knowledge of industry trends, emerging technologies and clinical best practice.
+ Serve as the modality expert for CT clinical applications across the region.
**What You'll Bring**
**Essential Qualifications & Experience**
+ Degree qualification in Medical Radiation Science (Diagnostic Radiography) or a related discipline.
+ Minimum 10 years' clinical experience in Computed Tomography.
+ Advanced expertise in CT clinical applications, protocols and workflow optimisation.
+ Experience leading teams, projects or clinical initiatives.
+ Strong stakeholder management and relationship-building capability.
+ Knowledge of the Australian and New Zealand healthcare and imaging landscape.
+ Excellent communication, presentation and influencing skills.
**Preferred**
+ Experience working with GE HealthCare CT systems.
+ Previous clinical applications, education or vendor experience.
+ Experience managing strategic clinical projects and customer programs.
+ Established project management capability.
+ Experience engaging with KOLs, professional societies or research organisations.
**Desired Characteristics**
We're looking for someone who is:
+ Passionate about clinical excellence and improving patient outcomes.
+ A natural collaborator who thrives in a matrix environment.
+ Strategic, consultative and customer-focused.
+ Highly organised with strong project management skills.
+ Analytical and solutions-oriented.
+ Comfortable influencing stakeholders at all levels.
+ Committed to continuous learning and innovation.
**Why GE Healthcare?**
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
+ Flexible working options
+ Competitive salary + bonus + car allowance
+ 5 weeks leave (ask about "take 5")
+ Generous leave & family policies
+ Long term career opportunities (locally and globally)
+ Generous discounts for goods & services via our employee benefits program (think travel, entertainment & shopping!) *This was recently rated as one of our employees favourite benefits!
**Vaccinations**
Access to healthcare sites requires compliance with applicable Vaccine Preventable Disease (VPD) requirements under state/territory health directives. You will be required to provide evidence of vaccination or immunity prior to site access, and on an ongoing basis as requirements evolve. Reasonable adjustments may be considered where a legitimate medical exemption applies.
**Additional Information**
**Relocation Assistance Provided:** No
At GE HealthCare, we are enabling precision care through innovative medical technologies, advanced imaging solutions and clinical intelligence.
We are seeking an experienced CT Clinical Insights Specialist to provide strategic clinical leadership across Australia and New Zealand. This highly influential role partners with customers, Key Opinion Leaders (KOLs), commercial teams and product specialists to drive clinical excellence, workflow optimisation and customer success across our Computed Tomography (CT) portfolio.
As a recognised CT expert, you will help shape clinical best practice, support commercial growth, advance customer adoption of innovative technologies and strengthen GE HealthCare's position as a trusted partner in diagnostic imaging.
**Job Description**
**About the Role**
The CT Clinical Insights Specialist role blends clinical expertise, customer engagement and commercial collaboration to deliver exceptional outcomes for healthcare providers throughout the ANZ region.
You will work closely with customers to optimise clinical protocols, improve workflow efficiency and support the adoption of advanced CT technologies. Additionally, you will play a key role in developing KOL relationships, supporting strategic projects and providing advanced clinical education to both customers and internal teams.
**Key Responsibilities**
**Clinical Leadership & Commercial Support**
+ Provide high-level clinical expertise during customer engagements, demonstrations and site visits.
+ Support strategic sales opportunities, large capital projects and tender submissions.
+ Demonstrate the clinical and operational value of GE HealthCare CT solutions.
+ Collaborate closely with Sales, Marketing, Service and Leadership teams to support business objectives and customer outcomes.
**Customer Success & Clinical Optimisation**
+ Partner with healthcare providers to optimise CT clinical protocols and workflow efficiency.
+ Identify opportunities to enhance clinical performance and improve operational outcomes.
+ Act as a trusted advisor to radiology leaders, clinicians and imaging departments.
+ Stay connected to evolving customer needs and emerging healthcare challenges.
**Key Opinion Leader & Market Development**
+ Develop and maintain relationships with leading CT clinicians and industry influencers across ANZ.
+ Support the development and ongoing success of reference and showcase sites.
+ Collaborate with KOLs on the evaluation of new techniques, clinical advancements and research initiatives.
+ Build relationships with academic institutions, professional societies and healthcare stakeholders.
+ Contribute to marketing initiatives and support execution of regional growth strategies.
**Education & Clinical Excellence**
+ Deliver advanced customer training and education programs.
+ Support the professional development of internal commercial and clinical teams.
+ Promote clinical differentiation and evidence-based value propositions across the CT portfolio.
+ Maintain expert knowledge of industry trends, emerging technologies and clinical best practice.
+ Serve as the modality expert for CT clinical applications across the region.
**What You'll Bring**
**Essential Qualifications & Experience**
+ Degree qualification in Medical Radiation Science (Diagnostic Radiography) or a related discipline.
+ Minimum 10 years' clinical experience in Computed Tomography.
+ Advanced expertise in CT clinical applications, protocols and workflow optimisation.
+ Experience leading teams, projects or clinical initiatives.
+ Strong stakeholder management and relationship-building capability.
+ Knowledge of the Australian and New Zealand healthcare and imaging landscape.
+ Excellent communication, presentation and influencing skills.
**Preferred**
+ Experience working with GE HealthCare CT systems.
+ Previous clinical applications, education or vendor experience.
+ Experience managing strategic clinical projects and customer programs.
+ Established project management capability.
+ Experience engaging with KOLs, professional societies or research organisations.
**Desired Characteristics**
We're looking for someone who is:
+ Passionate about clinical excellence and improving patient outcomes.
+ A natural collaborator who thrives in a matrix environment.
+ Strategic, consultative and customer-focused.
+ Highly organised with strong project management skills.
+ Analytical and solutions-oriented.
+ Comfortable influencing stakeholders at all levels.
+ Committed to continuous learning and innovation.
**Why GE Healthcare?**
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you'd expect from an organization with global strength and scale, and you'll be surrounded by career opportunities in a culture that fosters care, collaboration and support.
+ Flexible working options
+ Competitive salary + bonus + car allowance
+ 5 weeks leave (ask about "take 5")
+ Generous leave & family policies
+ Long term career opportunities (locally and globally)
+ Generous discounts for goods & services via our employee benefits program (think travel, entertainment & shopping!) *This was recently rated as one of our employees favourite benefits!
**Vaccinations**
Access to healthcare sites requires compliance with applicable Vaccine Preventable Disease (VPD) requirements under state/territory health directives. You will be required to provide evidence of vaccination or immunity prior to site access, and on an ongoing basis as requirements evolve. Reasonable adjustments may be considered where a legitimate medical exemption applies.
**Additional Information**
**Relocation Assistance Provided:** No
Is this job a match or a miss?
Apply Now
3
Regional Medical Oncology Fellow: Clinical Trials & Research
3350 Bakery Hill
Stawell Regional Health
Posted today
Job Viewed
Job Description
Job Description
Stawell Regional Health is seeking a Medical Oncology Fellow for the 2027 clinical year at the Ballarat Regional Integrated Cancer Centre (BRICC). This role is a 12-month fixed-term fellowship offering extensive clinical and research opportunities within a reputable regional oncology service.
You'll work with experienced consultants and participate in both patient care and clinical research, making a significant impact in regional medical practice.
Ideal candidates will have a medical qualification with oncology training, strong teamwork skills, and a focus on patient-centered care.
#J-18808-LjbffrIs this job a match or a miss?
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4
Job Description
Clinical Research Associate, Home-based in Australia
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
**CRA II / Senior CRA**
**Home-based in Australia**
We are currently seeking a Clinical Research Associates to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
**What you will be doing**
+ Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
+ Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
+ Collaborating with investigators and site staff to facilitate smooth study conduct.
+ Performing data review and resolution of queries to maintain high-quality clinical data.
+ Contributing to the preparation and review of study documentation, including protocols and clinical study reports
**Your profile**
+ Bachelor's degree in a scientific or healthcare-related field.
+ Minimum of 2 years of independent monitoring experience as a Clinical Research Associate within CRO/Pharma.
+ In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
+ Strong organizational and communication skills, with attention to detail.
+ Ability to work independently and collaboratively in a fast-paced environment.
+ Ability to travel locally and interstate and should possess a valid driver's license
\#LI-JS1
\#LI-Remote
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
**CRA II / Senior CRA**
**Home-based in Australia**
We are currently seeking a Clinical Research Associates to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies.
**What you will be doing**
+ Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
+ Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
+ Collaborating with investigators and site staff to facilitate smooth study conduct.
+ Performing data review and resolution of queries to maintain high-quality clinical data.
+ Contributing to the preparation and review of study documentation, including protocols and clinical study reports
**Your profile**
+ Bachelor's degree in a scientific or healthcare-related field.
+ Minimum of 2 years of independent monitoring experience as a Clinical Research Associate within CRO/Pharma.
+ In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
+ Strong organizational and communication skills, with attention to detail.
+ Ability to work independently and collaboratively in a fast-paced environment.
+ Ability to travel locally and interstate and should possess a valid driver's license
\#LI-JS1
\#LI-Remote
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
Is this job a match or a miss?
Apply Now
5
Job Description
Are you a **Clinical Research Associate** looking for your next big adventure?
Look no further than IQVIA, a global CRO with outstanding reputation.
Our CRA teams have current openings across various locations in Australia.
**The role:**
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
**Essential Functions**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
+ Collaborate and liaise with study team members for project execution support as appropriate.
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
**Qualifications**
+ Bachelor's Degree in scientific discipline or health care.
+ Requires at least 9 months of independent on-site monitoring experience.
+ Equivalent combination of education, training and experience may be accepted in lieu of degree.
+ Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
+ Good therapeutic and protocol knowledge as provided in company training.
+ Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
+ Organizational and problem-solving skills.
+ Effective time and financial management skills.
+ Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
+ Candidates will be assessed according to their years of experience and be considered for various levels where applicable.
**What's in it for you?**
+ Flexible hybrid work environment, with an office in the heart of Melbourne and Sydney.
+ Competitive salary with car and health allowances.
+ Career growth and opportunity across our FSO and FSP models.
+ Work with skilled Managers across multi-phases clinical trials
If you are interested and meet the skills and experience above, please apply with your resume today.
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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
Look no further than IQVIA, a global CRO with outstanding reputation.
Our CRA teams have current openings across various locations in Australia.
**The role:**
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
**Essential Functions**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
+ Collaborate and liaise with study team members for project execution support as appropriate.
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
**Qualifications**
+ Bachelor's Degree in scientific discipline or health care.
+ Requires at least 9 months of independent on-site monitoring experience.
+ Equivalent combination of education, training and experience may be accepted in lieu of degree.
+ Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
+ Good therapeutic and protocol knowledge as provided in company training.
+ Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
+ Organizational and problem-solving skills.
+ Effective time and financial management skills.
+ Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
+ Candidates will be assessed according to their years of experience and be considered for various levels where applicable.
**What's in it for you?**
+ Flexible hybrid work environment, with an office in the heart of Melbourne and Sydney.
+ Competitive salary with car and health allowances.
+ Career growth and opportunity across our FSO and FSP models.
+ Work with skilled Managers across multi-phases clinical trials
If you are interested and meet the skills and experience above, please apply with your resume today.
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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
Is this job a match or a miss?
Apply Now
6
Job Description
CRA II, Home-based in Australia
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
**Title: CRA II**
**Location: Australia**
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
**What You Will Do:**
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
+ Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
+ Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
+ Collaborating with investigators and site staff to facilitate smooth study conduct.
+ Performing data review and resolution of queries to maintain high-quality clinical data.
+ Contributing to the preparation and review of study documentation, including protocols and clinical study reports
**Your Profile:**
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
+ Bachelor's degree in a scientific or healthcare-related field.
+ **Minimum of 2 years of experience as a Clinical Research Associate within CRO/Pharma (mandatory)**
+ In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
+ Strong organizational and communication skills, with attention to detail.
+ Ability to work independently and collaboratively in a fast-paced environment.
+ Willingness to travel as required
\#LI-JS1
\#LI-Remote
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
**Title: CRA II**
**Location: Australia**
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
**What You Will Do:**
You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
+ Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
+ Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
+ Collaborating with investigators and site staff to facilitate smooth study conduct.
+ Performing data review and resolution of queries to maintain high-quality clinical data.
+ Contributing to the preparation and review of study documentation, including protocols and clinical study reports
**Your Profile:**
You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.
Required qualifications and experience:
+ Bachelor's degree in a scientific or healthcare-related field.
+ **Minimum of 2 years of experience as a Clinical Research Associate within CRO/Pharma (mandatory)**
+ In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
+ Strong organizational and communication skills, with attention to detail.
+ Ability to work independently and collaboratively in a fast-paced environment.
+ Willingness to travel as required
\#LI-JS1
\#LI-Remote
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
Is this job a match or a miss?
Apply Now
7
Job Description
**Job Overview**
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
**Essential Functions**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
+ Collaborate and liaise with study team members for project execution support as appropriate.
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
**Qualifications**
+ Bachelor's Degree in scientific discipline or health care.
+ Requires at least 1 year of on-site monitoring experience.
+ Equivalent combination of education, training and experience may be accepted in lieu of degree.
+ Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
+ Good therapeutic and protocol knowledge as provided in company training.
+ Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
+ Written and verbal communication skills including good command of English language.
+ Organizational and problem-solving skills.
+ Effective time and financial management skills.
+ Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
+ Candidates will be assessed according to their years of experience and be considered for various levels where applicable.
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements.
**Essential Functions**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
+ Collaborate and liaise with study team members for project execution support as appropriate.
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis.
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement.
**Qualifications**
+ Bachelor's Degree in scientific discipline or health care.
+ Requires at least 1 year of on-site monitoring experience.
+ Equivalent combination of education, training and experience may be accepted in lieu of degree.
+ Good knowledge of, and skill in applying, applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
+ Good therapeutic and protocol knowledge as provided in company training.
+ Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
+ Written and verbal communication skills including good command of English language.
+ Organizational and problem-solving skills.
+ Effective time and financial management skills.
+ Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
+ Candidates will be assessed according to their years of experience and be considered for various levels where applicable.
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
IQVIA 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
Is this job a match or a miss?
Apply Now
8
Job Description
Senior Site Partner - Home‑Based in Australia or New Zealand
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
**Role: Site Partner II (Study Start Up Associate II)**
**Location: Home-based in Australia**
We are currently seeking a Site Partner I/ II to join our diverse and dynamic team. As a Site Partner at ICON, you will act as a strategic liaison between ICON and key investigator sites, strengthening relationships and supporting excellent study performance. You will champion site needs internally while helping sites navigate ICON processes and studies across their portfolio.
**What You Will Be Doing:**
+ Building and maintaining strong, long-term relationships with key investigator sites, acting as their primary ICON point of contact.
+ Supporting sites across multiple studies by facilitating communication, addressing operational challenges, and escalating issues as needed.
+ Collaborating with clinical operations, feasibility, and project teams to align site capabilities with study opportunities.
+ Gathering and sharing site feedback and insights to inform protocol design, feasibility assumptions, and process improvements.
+ Monitoring performance metrics for partnered sites, including start-up timelines, recruitment, and quality, and driving improvement actions.
+ Contributing to site engagement strategies, tools, and best practices to enhance the overall site experience.
**Your Profile:**
+ Bachelor's degree in life sciences, healthcare, or a related field, or equivalent clinical research experience.
+ **Minimum 2+ years of SSU experience within CRO/Pharma**
+ Substantial experience in clinical research with strong exposure to site management, site partnerships, or site-facing roles.
+ Excellent relationship-building and stakeholder management skills, with credibility among investigators and site staff.
+ Good understanding of clinical trial operations, site processes, and key drivers of recruitment and quality.
+ Strong communication and problem-solving skills, with a proactive, solutions-oriented mindset.
+ Ability to manage multiple sites and studies in a matrixed environment while maintaining a high level of service and responsiveness.
\#LI-JS1
\#LI-Remote
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
**Role: Site Partner II (Study Start Up Associate II)**
**Location: Home-based in Australia**
We are currently seeking a Site Partner I/ II to join our diverse and dynamic team. As a Site Partner at ICON, you will act as a strategic liaison between ICON and key investigator sites, strengthening relationships and supporting excellent study performance. You will champion site needs internally while helping sites navigate ICON processes and studies across their portfolio.
**What You Will Be Doing:**
+ Building and maintaining strong, long-term relationships with key investigator sites, acting as their primary ICON point of contact.
+ Supporting sites across multiple studies by facilitating communication, addressing operational challenges, and escalating issues as needed.
+ Collaborating with clinical operations, feasibility, and project teams to align site capabilities with study opportunities.
+ Gathering and sharing site feedback and insights to inform protocol design, feasibility assumptions, and process improvements.
+ Monitoring performance metrics for partnered sites, including start-up timelines, recruitment, and quality, and driving improvement actions.
+ Contributing to site engagement strategies, tools, and best practices to enhance the overall site experience.
**Your Profile:**
+ Bachelor's degree in life sciences, healthcare, or a related field, or equivalent clinical research experience.
+ **Minimum 2+ years of SSU experience within CRO/Pharma**
+ Substantial experience in clinical research with strong exposure to site management, site partnerships, or site-facing roles.
+ Excellent relationship-building and stakeholder management skills, with credibility among investigators and site staff.
+ Good understanding of clinical trial operations, site processes, and key drivers of recruitment and quality.
+ Strong communication and problem-solving skills, with a proactive, solutions-oriented mindset.
+ Ability to manage multiple sites and studies in a matrixed environment while maintaining a high level of service and responsiveness.
\#LI-JS1
\#LI-Remote
**What ICON can offer you:**
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
+ Various annual leave entitlements
+ A range of health insurance offerings to suit you and your family's needs.
+ Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
+ Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
+ Life assurance
+ Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
Visit our careers site ( to read more about the benefits ICON offers.
At ICON, inclusion & belonging are fundamental to our culture and values. We're dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here ( in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there's every chance you're exactly what we're looking for here at ICON whether it is for this or other roles.
Are you a current ICON Employee? Please click here ( to apply
Is this job a match or a miss?
Apply Now
9