Clinical Project Manager Jobs
Clinical Project Manager jobs are open across pharmaceutical, biotech, medical device, and CRO sectors, from associate to senior and director level, with specializations in oncology trials, regulatory affairs, and global study management. Find a role that fits from the openings below and apply directly.
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Location: Parsippany, United States of America
Job Type: Full time
Work Arrangement: Home-based
IQVIA Biotech is seeking a Sr. Clinical Project Manager with experience in the following therapeutics: Cardiovascular, Renal, and Metabolic.
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.
Overview
The Senior Clinical Project Manager is a key leader in the delivery of clinical trials, partnering with cross-functional teams and clients to accelerate the development of life-changing therapies. This role is responsible for end-to-end clinical study execution, ensuring projects are delivered on time, within scope, and on budget, while maintaining the highest standards of quality and compliance. The Senior Clinical Project Manager provides strategic oversight, operational leadership, and serves as the primary point of contact for sponsors.
Key Responsibilities
- Lead the planning, execution, and delivery of medium to large, multi-regional clinical studies in alignment with contractual requirements, SOPs, and regulatory standards.
- Develop and implement integrated study management plans, ensuring consistency in processes, tools, and training.
- Serve as the primary liaison with sponsors, building strong client relationships and ensuring transparent communication on project status, risks, and deliverables.
- Set direction and objectives for cross-functional project teams; monitor performance and drive accountability to meet milestones.
- Partner with Business Development on bid defenses and contribute to winning new business, including leading presentations when applicable.
- Proactively identify, assess, and mitigate risks; lead issue resolution and implement corrective and preventative action plans.
- Collaborate with internal functional groups to support study execution and overcome operational challenges.
- Monitor project progress against timelines, budget, and quality metrics; provide regular updates to internal and external stakeholders.
- Ensure financial performance by managing budgets, forecasting revenue, and identifying opportunities to accelerate delivery.
- Manage scope changes and oversee change control processes in collaboration with stakeholders.
- Promote continuous improvement by sharing lessons learned and best practices.
- Mentor and support the development of junior team members and contribute feedback on team performance.
Qualifications
- Bachelor’s Degree in Life Sciences or a related field required; advanced degree preferred.
- Requires greater than 7 years of clinical research experience, including at least 4 years of project management experience, or an equivalent combination of education, training, and experience.
- Proven ability to manage complex, global clinical trials and cross-functional teams.
- Strong leadership, communication, and stakeholder management skills.
- Demonstrated ability to manage budgets, timelines, and risk proactively.
- Experience leading bid defenses and client engagements is preferred.
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.
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.
Location: Parsippany, United States of America
Job Type: Full time
Work Arrangement: Home-based
IQVIA Biotech is seeking a Sr. Clinical Project Manager with experience in the following therapeutics: Cardiovascular, Renal, and Metabolic.
IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.
Overview
The Senior Clinical Project Manager is a key leader in the delivery of clinical trials, partnering with cross-functional teams and clients to accelerate the development of life-changing therapies. This role is responsible for end-to-end clinical study execution, ensuring projects are delivered on time, within scope, and on budget, while maintaining the highest standards of quality and compliance. The Senior Clinical Project Manager provides strategic oversight, operational leadership, and serves as the primary point of contact for sponsors.
Key Responsibilities
- Lead the planning, execution, and delivery of medium to large, multi-regional clinical studies in alignment with contractual requirements, SOPs, and regulatory standards.
- Develop and implement integrated study management plans, ensuring consistency in processes, tools, and training.
- Serve as the primary liaison with sponsors, building strong client relationships and ensuring transparent communication on project status, risks, and deliverables.
- Set direction and objectives for cross-functional project teams; monitor performance and drive accountability to meet milestones.
- Partner with Business Development on bid defenses and contribute to winning new business, including leading presentations when applicable.
- Proactively identify, assess, and mitigate risks; lead issue resolution and implement corrective and preventative action plans.
- Collaborate with internal functional groups to support study execution and overcome operational challenges.
- Monitor project progress against timelines, budget, and quality metrics; provide regular updates to internal and external stakeholders.
- Ensure financial performance by managing budgets, forecasting revenue, and identifying opportunities to accelerate delivery.
- Manage scope changes and oversee change control processes in collaboration with stakeholders.
- Promote continuous improvement by sharing lessons learned and best practices.
- Mentor and support the development of junior team members and contribute feedback on team performance.
Qualifications
- Bachelor’s Degree in Life Sciences or a related field required; advanced degree preferred.
- Requires greater than 7 years of clinical research experience, including at least 4 years of project management experience, or an equivalent combination of education, training, and experience.
- Proven ability to manage complex, global clinical trials and cross-functional teams.
- Strong leadership, communication, and stakeholder management skills.
- Demonstrated ability to manage budgets, timelines, and risk proactively.
- Experience leading bid defenses and client engagements is preferred.
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.
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.
See All 486+ Clinical Project Manager Jobs
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Find Clinical Project Manager JobsClinical Project Manager Job Market
A snapshot from current openings nationwide, updated as new roles post.
Who's Hiring
- Medpace123
- Genentech35
- IQVIA18
- Syneos Health14
- Revolution Medicines11
Top Industries Hiring
- Biotechnology & Pharmaceuticals160
- Healthcare & Medical Services140
- Science & Research93
- Education56
- Consulting & Professional Services44
What Employers Look For
The qualifications that appear most often in clinical project manager jobs.
- Bachelor's degree in life sciences, nursing, or a related field
- Direct experience managing Phase I through Phase III clinical trials
- Proficiency with CTMS and EDC platforms such as Medidata or Veeva
- Project Management Professional or Clinical Research Associate certification preferred
- Strong knowledge of ICH-GCP guidelines and FDA regulatory requirements
- Experience overseeing CRO relationships, budgets, and site performance
Tips for Your Clinical Project Manager Job Search
Quantify your trial portfolio on your resume
List the number of clinical trials you've managed, their phases, and therapeutic areas. Hiring managers scan for Phase II and Phase III experience first, so put those details in your summary and in each role's bullet points.
Highlight your clinical systems proficiency
Call out specific platforms you've used: CTMS, EDC systems like Medidata Rave or Veeva Vault, and eTMF tools. Many job postings filter candidates early on system familiarity, so naming tools directly beats vague phrases like 'data management experience.'
Apply early to roles that fit
Migrate Mate lists clinical project manager openings from across the United States in one place, so you can find roles that match and apply directly to each listing.
Target postings by trial phase and indication
Search for openings that match your actual study experience. If you've led oncology Phase II trials, filter for those terms. Applying to roles that match your therapeutic background makes your resume far more relevant to the hiring team.
Prepare for budget and vendor management questions
Interviewers for clinical project manager roles routinely ask how you've managed CRO relationships and study budgets. Prepare two or three specific examples that show how you handled scope changes, vendor delays, or cost overruns without derailing timelines.
Follow up with the hiring team after your interview
Send a brief note within 24 hours that references a specific topic from your conversation, such as a protocol challenge you discussed. Clinical project manager roles involve constant stakeholder communication, and a focused follow-up demonstrates exactly that skill.
Clinical Project Manager Jobs: Frequently Asked Questions
Which companies are hiring the most clinical project managers?
The companies hiring the most clinical project managers right now include Medpace, Genentech, and IQVIA, with the largest share of openings in Ohio, California, and Colorado, based on current listings on Migrate Mate as of June 2026. Demand is especially high at large CROs and mid-size biotech companies running active oncology and rare disease programs.
How many clinical project manager jobs are remote?
About 24% of clinical project manager openings are fully remote or hybrid as of June 2026, making it one of the more location-flexible roles in the clinical operations field. Roles focused on study management, vendor oversight, and cross-functional coordination tend to be the most remote, while positions that require frequent site visits or on-site sponsor work are typically hybrid or on-site.
How do you become a clinical project manager?
Most clinical project managers start as clinical research associates or study coordinators, building hands-on trial experience before moving into a management role. Earning a GCP certification or a PMP credential strengthens your candidacy. From there, you take on increasing responsibility for full study oversight, vendor relationships, and cross-functional team leadership until you're ready to step into a CPM title.
Can you get a clinical project manager job with limited experience?
Yes, but you'll need to position your application carefully. Roles titled associate clinical project manager or junior CPM are designed for candidates with one to three years of clinical research experience. Emphasize any exposure to trial timelines, protocol deviations, or site communications in your current or past roles, and highlight a GCP certification or relevant coursework to close credential gaps.
What does the clinical project manager interview process look like?
Most clinical project manager interview processes include an initial recruiter screen, a hiring manager interview focused on your trial experience and leadership style, and a final panel with cross-functional stakeholders such as data management, regulatory, or clinical operations leads. Expect behavioral questions about managing competing priorities across multiple studies, handling difficult CRO relationships, and keeping trials on timeline when unexpected protocol issues arise.
Where can I find and apply to clinical project manager jobs?
You can find and apply to clinical project manager jobs on Migrate Mate, which lists current openings from across the United States. Search the listings to find roles that match your trial experience and therapeutic background, then apply directly to each one that fits.
See All 486+ Clinical Project Manager Jobs
Jump back to the full list of openings and apply to any clinical project manager role that fits.
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