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Senior Clinical Project Manager Jobs (NOW HIRING)

$93 - $233/hr

Senior Clinical Project Manager - Global Study Leadership At IQVIA, our Senior Project Managers play a pivotal role in bringing innovative medicines to patients worldwide. You'll provide strategic ...

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$52K

$115.6K

$201K

How much do senior clinical project manager jobs pay per year?

As of Sep 5, 2026, the average yearly pay for senior clinical project manager in the United States is $115,579.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,500.00 and $143,000.00 per year, depending on experience, location, and employer.

What is a senior clinical project manager?

A Senior Clinical Project Manager is a professional responsible for overseeing and managing clinical trials and research projects within the pharmaceutical, biotechnology, or medical device industries. They coordinate all aspects of a clinical study, including planning, execution, budgeting, and compliance with regulatory requirements. Senior Clinical Project Managers lead cross-functional teams, communicate with stakeholders, and ensure that clinical trials are completed on time, within scope, and according to quality standards. Their expertise is crucial for the successful development of new treatments and therapies.

What does a senior clinical project manager do?

As a senior clinical project manager, your responsibilities center around the management of a clinical trial team. You assign projects, ensure the success of team activities, and enforce company regulations. Your duties include staying within the scope of a budget while carrying out a clinical trial. You manage your team through each study as you plan out their responsibilities, keeping the project on track and cost-effective. As a senior clinical project manager, you create reports on the efficiency and progress of each clinical trial.

What are the key skills and qualifications needed to thrive as a senior clinical project manager?

To thrive as a Senior Clinical Project Manager, you need in-depth knowledge of clinical research, regulatory requirements, project management methodologies, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as PMP or equivalent are commonly required. Strong leadership, problem-solving, and communication skills help manage cross-functional teams and stakeholder expectations. These skills and qualifications ensure efficient trial execution, regulatory compliance, and the successful delivery of clinical projects within timelines and budgets.

How does a senior clinical project manager typically collaborate with cross-functional teams throughout a clinical trial?

A Senior Clinical Project Manager plays a pivotal role in coordinating cross-functional teams, such as clinical operations, data management, biostatistics, regulatory affairs, and vendors. They facilitate regular meetings, ensure effective communication, and resolve any interdepartmental issues that may arise during the study. By fostering collaboration and aligning team objectives, they help maintain timelines, manage resources, and ensure the trial progresses smoothly and compliantly. This collaborative approach is essential for the successful execution and delivery of clinical projects.

What is the difference between Senior Clinical Project Manager vs Clinical Project Manager?

AspectSenior Clinical Project ManagerClinical Project Manager
Required CredentialsTypically requires 5+ years of experience, advanced certifications (e.g., PMP), and strong leadership skillsUsually requires 2-4 years of experience, relevant certifications, and foundational project management skills
Work EnvironmentLeads multiple projects, manages teams, and interacts with senior stakeholdersManages individual projects, coordinates with teams, and reports to senior managers
Employer & Industry UsageCommonly employed in pharmaceutical, biotech, and CRO companies for complex projectsUsed across similar industries for managing clinical trials at various scales

The main difference between a Senior Clinical Project Manager and a Clinical Project Manager lies in experience, leadership responsibilities, and project scope. Senior roles involve overseeing multiple projects and guiding teams, while Clinical Project Managers focus on managing specific clinical trials. Both roles require relevant certifications and industry experience, but the senior position demands more strategic oversight and leadership skills.

What cities are hiring for Senior Clinical Project Manager jobs?

Cities with the most Senior Clinical Project Manager job openings:

Who are the top companies hiring for Senior Clinical Project Manager jobs?

The top employers for Senior Clinical Project Manager jobs are:

What states have the most Senior Clinical Project Manager jobs?

States with the most job openings for Senior Clinical Project Manager jobs include:

Infographic showing various Senior Clinical Project Manager job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 12% Part Time, and 1% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $115,579 per year, or $55.6 per hour.

Senior Clinical Project Manager (CAR-T)

IQVIA LLC

Durham, NC • On-site

$93 - $233/hr

Other

Posted 23 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services


Job description

Senior Clinical Project Manager - Global Study Leadership

At IQVIA, our Senior Project Managers play a pivotal role in bringing innovative medicines to patients worldwide. You'll provide strategic leadership for complex global clinical trials, partnering directly with sponsors and cross-functional teams to deliver studies that accelerate the development of life-changing therapies. This is an opportunity to lead large-scale, multi-regional studies for some of the world's most innovative pharmaceutical and biotechnology companies while expanding your leadership impact and helping shape the future of clinical research.

Why Join Global Study Leadership?

Global Study Leadership is a global, full-service team delivering clinical trials through both therapeutically aligned and customer-dedicated delivery models. You'll work on some of the industry's most complex global clinical trials, partnering directly with leading pharmaceutical and biotechnology sponsors across therapeutic areas including Oncology, Rare Disease, CNS, Cardiovascular, Immunology, Respiratory, Cell & Gene Therapy, Infectious Disease, Ophthalmology and Women's Health. Supported by a collaborative global network, flexible ways of working and AI-enabled technology and data-driven insights, you'll have exceptional opportunities to broaden your expertise, expand your leadership impact and accelerate your career within one of the world's leading clinical research organizations.

What You'll Be Doing
  • Lead the delivery of complex global and multi-regional clinical studies, driving operational excellence and successful study outcomes
  • Serve as the primary strategic partner for sponsors, providing leadership, guidance and innovative solutions to drive successful study outcomes
  • Provide leadership and direction to cross-functional teams across regions, fostering collaboration, accountability and high performance
  • Oversee study timelines, budgets, quality, risks, financial performance and operational delivery to ensure study success
  • Drive proactive risk management, issue resolution, decision-making and stakeholder alignment throughout the study lifecycle
  • Ensure studies are delivered in compliance with ICH-GCP, regulatory requirements and contractual commitments
What We're Looking For
  • Bachelor's degree in Life Sciences, Healthcare or a related scientific discipline
  • 7+ years of clinical research experience, including significant project management experience leading global or multi-regional clinical trials within a CRO, pharmaceutical or biotechnology environment
  • Strong knowledge of clinical trial conduct, ICH-GCP guidelines and applicable regulatory requirements
  • Proven success leading cross-functional teams and managing study delivery, including timelines, budgets, quality, risks and operational performance
  • Demonstrated ability to build trusted sponsor relationships and effectively manage senior stakeholders in a global environment
  • Exceptional leadership, communication, problem-solving and decision-making skills
  • Passion for advancing clinical research and improving patient outcomes
Build Your Future with IQVIA

If you're looking for a role that combines global exposure, strategic leadership, sponsor partnership and meaningful work, we'd love to hear from you. At IQVIA, you'll have the opportunity to work on high-profile global studies, collaborate with industry-leading sponsors, leverage cutting-edge technology and build a rewarding career with one of the world's leading clinical research organizations, all while helping bring innovative treatments to patients faster.

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 proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law.

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.

The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time).

  • Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere.

Thank you for your interest in growing your career with us.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US