1,000+ matching jobs for “Clinical Research Associate”

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IQVIA Holdings

Associate Director, Clinical Project Management

Kuala Lumpur, Malaysia

… with the core project team. Accountable for the strategic development and execution or delivery of clinical studies in line with agreed upon contracts while optimizing speed, quality and cost of delivery, ensuring …

Added Oct 15, 2026

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McKesson

Research Nurse

Denver, Colorado, United States

Pay posted by employer$83,000–$100,000 per year

… It’s a Mission. Our people are the foundation of our success. By joining our growing team at Sarah Cannon Research Institute (SCRI), a subsidiary of McKesson, you will have the opportunity to become part of one of the …

Added Oct 27, 2026

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Merck (MSD)

Biologics Process Research & Development, Associate Scientist

Rahway, New Jersey, United States

Pay posted by employer$71,900–$113,200

Our Research Scientists are our Inventors. Using innovative thinking, state-of-the-art facilities, and robust …

Added Oct 16, 2026

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Thermo Fisher Scientific

FSP Experienced Clinical Research Associate (CRA II/Sr. CRA I) - Oncology - Respiratory - Cardiovascular - US West

Remote, Oregon, USA

Join us as a Clinical Research Associate II/Sr. Clinical Research Associate I- Make an impact at the Forefront of Innovation. We have successfully …

Added Oct 16, 2026

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Merck (MSD)

Executive Director, Product Development Team Leader, Clinical Research, Hematology - Lymphoma

Rahway, New Jersey, United States +2 locations

Pay posted by employer$310,900–$489,400

… and Product Development Team (PDT) lead has primary responsibility for the planning and directing of clinical research activities involving new or marketed medicines in the Oncology therapeutic area, Hematology …

Added Oct 18, 2026

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IQVIA Holdings

Associate/Clinical Project Manager (Client Dedicated)

Seoul, Republic of Korea

supporting the efforts of the Clinical Project Manager to drive operational excellence and strategic leadership with our customers. Associate …

Added Oct 15, 2026

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Johnson & Johnson

Associate Medical Director, Clinical Science Immunology

Chiyoda, Japan

Full time
Regular

… patients every step of the way. Learn more at https://www.jnj.com/innovative-medicine JOB SUMMARY: Associate Medical Directo r (AMD) assumes the role of Japan Study Responsible Physician (SRP) and is accountable for …

Added Oct 15, 2026

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Vertex Pharmaceuticals

Clinical Development Associate Medical Director- Pain

Boston, Massachusetts, United States

Full time
Regular

Pay posted by employer$204,000–$306,000

General Summary: The Clinical Development Associate Medical Director will serve as the Medical Lead for clinical trials, working with …

Added Oct 27, 2026

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Vertex Pharmaceuticals

Clinical Development Associate Medical Director-Nephrology

Boston, Massachusetts, United States

Full time
Regular

Pay posted by employer$204,000–$306,000

General Summary: The Clinical Development Associate Medical Director will serve as the Medical Lead for clinical trials, working with …

Added Oct 18, 2026

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Vertex Pharmaceuticals

Clinical Development Associate Medical Director- gMG

Boston, Massachusetts, United States

Full time
Regular

Pay posted by employer$204,000–$306,000

General Summary: The Clinical Development Associate Medical Director will serve as the Medical Lead for clinical trials, working with …

Added Oct 18, 2026

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Amgen

Senior Associate Clinical Trials Regulatory Affairs

Switzerland - Rotkreuz

Full time
Regular

… that read over 10 million patients worldwide. It’s time for a career you can be proud of. Join us. SENIOR ASSOCIATE CLINICAL TRIALS REGULATORY AFFAIRS LIVE What you will do In this vital role as Senior Associate Clinical …

Added Oct 15, 2026

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Thermo Fisher Scientific

Experienced Clinical Research Associate (CRA II / SR CRA I / SR CRA II) - US West - FSO

Remote, California, USA

Pay posted by employer$84,000–$120,000

Join Us as an Experienced Clinical Research Associate – Make an Impact at the Forefront of Innovation We have successfully supported the top 50 pharmaceutical …

Added Oct 16, 2026

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IQVIA Holdings

Associate/Clinical Project Manager, Sponsor Dedicated

Seoul, Republic of Korea

… requirements. Partners with the Clinical Trial Assistant (CTA)/Investigator Document Assistant (IDA), Clinical Research Associate (CRA) and Central Trial Manager (CTM)/Global Trial Manager to ensure overall study delivery at the country …

Added Oct 15, 2026

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IQVIA Holdings

Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated

Montréal, Canada +1 location

Pay posted by employer$73,600–$182,500

… 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, …

Added Oct 15, 2026

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IQVIA Holdings

Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated

Kirkland, Canada

Pay posted by employer$74,700–$154,000

Added Oct 15, 2026

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IQVIA Holdings

Associé(e) de recherche clinique (ARC) principal(e) / Senior Clinical Research Associate, Sponsor Dedicated

Mississauga, Canada

Pay posted by employer$102,500–$136,700

Added Oct 15, 2026

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Regeneron Pharmaceuticals

Associate Director, Clinical Scientist, Genetics Medicine

TARRYTOWN

Full time
Regular

Pay posted by employer$176,100–$287,300

… and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Clinical Sciences to join our Clinical Development Unit, supporting our clinical programs in a …

Added Oct 16, 2026

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Regeneron Pharmaceuticals

Associate Director Precision Medicine - Clinical Diagnostics

Remote - United States

Full time
Regular

Pay posted by employer$176,100–$287,300

Build our future together: We're seeking an Associate Director to lead companion diagnostic (CDx) strategy and development, bridging translational science with …

Added Oct 15, 2026

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Merck (MSD)

Associate Director, Regional Clinical Liaison, Marketing

USA - Pennsylvania - North Wales (Upper Gwynedd) +5 locations

Pay posted by employer$173,200–$272,600

Title: Associate Director, Regional Clinical Liaison - HIV Treatments (U.S.) Our company has been committed to advancing …

Added Oct 16, 2026

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Thermo Fisher Scientific

Principal Clinical Research Associate (PCRA) / Klinischer Monitor – Full-Time or Part-Time Available (m/w/d)

Remote, Germany +12 locations

… or Part-time (32 hours/week) options available About the Role We are seeking a highly experienced Principal Clinical Research Associate (CRA) to lead and coordinate all aspects of clinical monitoring and site management for complex clinical …

Added Oct 16, 2026

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IQVIA Holdings

Associate Director, Clinical Project Management

Kuala Lumpur, Malaysia

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Qualifications · employer excerpt

Bachelor's Degree Life sciences or related field
Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience.
Requires 10 years clinical research experience including 6 years of project management experience or equivalent combination of education, training and experience. Req
Knowledge of clinical trials - Knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial…
Communication - Strong written and verbal communication skills including good command of English language Strong presentation skills. Requires strong negotiation and customer management skills.

11 more in the full description below.

About this opportunity

Original employer description

Manage and support the operational elements and execution of studies and/or programs to ensure delivery; time and quality resulting in strong financial performance and customer satisfaction and in accordance with SOPs; policies and practices from pre-award to close-out. Work with study(ies)/program(s) teams to focus on leveraging deep therapeutic expertise and IQVIA solutions to drive operational excellence and strategic leadership with our customers.

Essential Functions

Participate in bid defense preparations. Lead bid defense presentations in partnership with Business Development for large sized, multiple and full service, multiple country and/or multi regional studies. Understand project strategy and operationalise the agreed upon approach.
Develop and/or support on the preparation of integrated study management plans in collaboration with the core project team.
Accountable for the strategic development and execution or delivery of clinical studies in line with agreed upon contracts while optimizing speed, quality and cost of delivery, ensuring consistent use of study tools and training materials and compliance with system updates, standard processes, policies and procedures.
Serve as primary project oversight and/or contact with customers and own relationship with the project’s key customer contact(s), communicate/collaborate with IQVIA business development representatives as necessary.;
Set objectives for the core project team according to agreed upon contract, strategy and approach, effectively communicate and assess performance, providing feedback and leadership.
Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
Monitor progress against contract and prepare/present project information proactively to all stakeholders internally and externally.
Supervise problem solving and resolution efforts to include management of risk, contingencies and issues. Take accountability for proactive contingency plans to mitigate risks.
Coach and/or mentor junior team members around project delivery, planning, project review, risk management and problem solving to ensure global alignment of work practices across the team.
Achieve project quality by identifyingand proactively managing quality risks and issues, responding to issues raised by project team members and planning/implementing appropriate corrective and preventative action plans.
May participate in executive committees as part of program leadership.
Ensure the financial success of the project including optimal management and assignment of resources to achieve project goals and profitability.
Forecast and identify opportunities to accelerate activities to bring milestones and revenue forward, implement appropriate actions to achieve.;
Identify changes in scope and manage change control process, including securing customer agreement to financial and milestone updates as necessary.
Identify and communicate lessons learned and best practices to promote continuous improvement.
Adopt corporate initiatives and changes, and serve as a change advocate when necessary.
Provide input to line managers on their project team members’ performance relative to project tasks. Support staff development.
Mentor less experienced project team members on assigned projects to support their professional development.

Qualifications

Bachelor's Degree Life sciences or related field
Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience.
Requires 10 years clinical research experience including 6 years of project management experience or equivalent combination of education, training and experience. Req
Knowledge of clinical trials - Knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge, therapeutic knowledge desired. Good understanding of the competitive environment and how to communicate/demonstrate value through IQVIA solutions.;
Communication - Strong written and verbal communication skills including good command of English language Strong presentation skills. Requires strong negotiation and customer management skills.
Problem solving - Strong problem solving skills.
Leadership - Ability to work through others to deliver results to the appropriate quality and timeline metrics, monitoring/managing performance and providing feedback, experience productively partnering cross functionally and with customers to advance work effectively and efficiently. Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.
Organisation - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.
Prioritisation - Ability to handle conflicting priorities. Ability to work strategically to realize project goals, identifying and developing positive and compelling visions for the successful delivery of the project.
Quality - Attention to detail and accuracy in work.
Quality - Results-oriented approach to work delivery and output. Demonstrated learning agility and openness to learning and keeping own knowledge and skill set current and evolving.
IT skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.
Collaboration - Ability to establish and maintain effective working relationships with co-workers, managers and clients. Excellent customer service skills and demonstrated ability to understand customer needs. Effective mentoring and training skills, fostering learning and knowledge sharing with colleagues.
Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences Good understanding of other IQVIA functions and their inter-relationship with Project Leadership.
Finances - Good understanding of project financials including experience managing, contractual obligations and implications.
IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, Innovation and Ownership).

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 https://jobs.iqvia.com

IQVIA 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.

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