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Clinical Project Manager Jobs (NOW HIRING)

Our FSO team is seeking an Cell & Gene Therapy Clinical Project Manager to join our growing team. This role requires 2 + years of global project management experience , with experience in cell & gene ...

RWE Clinical Project Manager

Durham, NC · On-site

$93K - $232K/yr

In this role, the clinical project manager will be responsible for end-to-end project delivery of real-world observational studies within the oncology therapeutic area. It is important for this ...

Our FSO team is seeking an Cell & Gene Therapy Clinical Project Manager to join our growing team. This role requires 2 + years of global project management experience , with experience in cell & gene ...

... project manager in healthcare, strongly preferred * Bachelor's Degree or higher required * PMP required * Clinical licensure or relevant clinical credential required (e.g. RN, LVN, ARRT, RRT/CRT ...

... project manager in healthcare, strongly preferred * Bachelor's Degree or higher required * PMP required * Clinical licensure or relevant clinical credential required (e.g. RN, LVN, ARRT, RRT/CRT ...

Our FSO team is seeking an Ophthalmology Senior Clinical Project Manager or Clinical Project Manager II to join our growing team. This role requires 3 + years of global project management experience ...

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Clinical Project Manager information

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How much do clinical project manager jobs pay per hour?

As of Jun 25, 2026, the average hourly pay for clinical project manager in the United States is $60.70, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $71.15 per hour, depending on experience, location, and employer.

What is the movie clinical about?

There is no widely known movie titled 'Clinical.' If referring to a film with a similar name, it may involve themes related to medical or psychological settings. As a Clinical Project Manager, understanding media related to healthcare can help in patient engagement and communication strategies, but the role primarily focuses on managing clinical trials and ensuring regulatory compliance.

What is the difference between Clinical Project Manager vs Clinical Research Associate?

AspectClinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMPUsually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors and sitesMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageFound in pharmaceutical, biotech, and CRO companies overseeing entire projectsPrimarily employed by CROs and sponsors to monitor trial sites

The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

What Does a Clinical Project Manager Do?

A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.

What are the key skills and qualifications needed to thrive as a Clinical Project Manager, and why are they important?

To thrive as a Clinical Project Manager, you need expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.

What does it mean for someone to be clinical?

In the context of a Clinical Project Manager, being clinical relates to working within the healthcare or medical research field, often overseeing clinical trials or studies involving patient data and medical interventions. It requires understanding clinical protocols, regulatory requirements, and collaborating with healthcare professionals. Strong organizational skills and knowledge of Good Clinical Practice (GCP) are essential for success in this role.

What is a clinical job?

A clinical job involves working directly with patients or in healthcare settings to support diagnosis, treatment, or research. Roles such as Clinical Project Managers oversee clinical trials, coordinate teams, ensure compliance with regulations, and manage project timelines using tools like electronic data capture systems. These positions often require relevant certifications and a strong understanding of medical protocols.

What does a Clinical Project Manager do?

A Clinical Project Manager oversees the planning, execution, and completion of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They coordinate teams, manage budgets, timelines, and ensure that studies comply with regulatory standards and company protocols. Clinical Project Managers act as the main point of contact between sponsors, vendors, and clinical research sites, working to ensure that trials progress smoothly and data integrity is maintained. Their role is critical in bringing new therapies and treatments to market safely and efficiently.

What are some common challenges Clinical Project Managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.

What do we mean by clinical?

In the context of a Clinical Project Manager, 'clinical' refers to activities related to the development, testing, and approval of medical treatments, drugs, or devices. It involves overseeing clinical trials, ensuring compliance with regulatory standards, and managing study teams to gather safety and efficacy data.
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What states have the most Clinical Project Manager jobs? States with the most job openings for Clinical Project Manager jobs include:

Clinical Project Manager II

Fortrea

On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


Fortrea rating

7.2

Company rating: 7.2 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

45th of 57 rated research


Job description

Our FSO team is seeking an Cell & Gene Therapy Clinical Project Manager to join our growing team. This role requires 2+ years of global project management experience, with experience in cell & gene therapy. Candidates must be based in the United States.
Job Overview:
Project Managers own the operational strategy, determining the most cost effective and efficient means to successfully run and complete projects on time, while maintaining quality, remaining within budget, while meeting the customer's needs and adhering to the contract. Project Managers will work to develop and lead high performing teams by collaborating with key stakeholders to manage all aspects of the end-to-end lifecycle of the project including scope, timelines, risk, and budget. A successful Project Manager will bring innovation and future focused approaches to clinical trials with a focus on patient centricity and consistent solutions-oriented delivery.
Summary of Responsibilities:
  • Take accountability for proactively driving project performance toward contracted deliverables while meeting customer needs and maintaining operational excellence.
  • Take ownership of the customer relationship while drawing on the Company's pool of experts.
  • Drive communication and collaboration with the client and project team across a matrixed, multi-cultural, environment. Lead the development of the project strategy and ensure prioritization with the project team and key stakeholders in the creation of clear, data driven strategies and proactive management of project scope, timelines, quality, and budget. In collaboration with relevant departments, prepare and deliver presentations for new business as required.
  • Lead the identification of project, financial and quality risk leveraging end to end risk management practices and quality by design principles. Appropriately utilize data sources, dashboards, and risk management strategies to drive innovation and proactive problem solving with the project and client teams. Lead the adherence to project governance and issue escalation pathways, ensuring that project plans are in place to address identified risk while adhering to professional standards, SOPs, client, and regulatory requirements.
  • Partner with project team members and key stakeholders to oversee and manage project budgets, resources, and scope. Ensure adherence to established budget and financial milestones. Accountable for accurately forecasting project revenue and managing project costs in adherence to the budget. Leading the timely management of changes to scope and the change order process. Ensures project team awareness and tracking of KPIs for any client specific metrics.
  • Provide inspiring leadership and play a key role in the creation of high performing project teams. Facilitating communication and teamwork while driving delivery, ensuring that team members understand contracted scope, timelines, and budget. Ensures that resource projections are accurate and visible to resourcing teams, proactively escalating resource constraints and challenges. Develops and mentors team members in multiple areas of expertise and provides feedback as needed to respective line managers.
  • All other duties as needed or assigned.

Qualifications (Minimum Required):
  • University/college degree (life science preferred) or certification in a related allied health profession (i.e., nursing, medical or laboratory technology) from an appropriately accredited institution.
  • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

Experience (Minimum Required):
  • Minimum of five (5) years of relevant clinical research experience in a pharmaceutical company/CRO.
  • 2+ years of Clinical Project Management experience within a CRO or pharma company
  • Experience working on Cell & Gene Therapy studies
  • Experience working with Biotech clients
  • In lieu of the above requirement, candidates with (a) six (6) years supervisory experience in a heath care setting and (b) five (5) years clinical research experience including one (1) years of project management experience (international clinical trial management experience preferred) in the pharmaceutical or CRO industries will be considered
  • Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
  • Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access, and Power Point).
  • Experience managing projects in a matrix and virtual environment.
  • Excellent communication, planning, and organizational skills.
  • Demonstrated ability to lead by example and to encourage team members to seek solutions independently.
  • Demonstrated ability to handle multiple competing priorities and to utilize resources effectively.
  • Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system.
  • Financial awareness and ability to actively utilize financial tracking systems.
  • Ability to work independently and mentor junior project team members.
  • Ability to negotiate and liaise with clients in a professional manner.
  • Ability to present to staff at all levels.

Preferred Qualifications Include:
  • Master's or other advanced degree.
  • PMP certification

What do you get?
Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:
  • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)
  • 401(K)
  • Paid time off (PTO) - Flex Plan
  • Employee recognition awards
  • Multiple ERG's (employee resource groups)
  • Target Pay Range (based on title): $ 125 - 135k

#LI - Remote
Applications will be accepted on an ongoing basis
Physical Demands/Work Environment:
  • Standard Office Environment or remote based work required.
  • Weekend and off-hour work as required.

Travel Requirements:
  • Local, Domestic, Regional, Global

Identify the expected travel requirements of the position on an annual basis:
  • % of time: up to 30%
  • % of the above that requires overnight stay: up to 30%
  • Travel is primarily to where: domestic and international travel

Learn more about our EEO & Accommodations request here.