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Contract Clinical Project Manager Jobs (NOW HIRING)

Fortrea

Clinical Project Manager II

Durham, NC · On-site

Our FSO team is seeking an Cell & Gene Therapy Clinical Project Manager to join our growing team ... to the contract. Project Managers will work to develop and lead high performing teams by ...

Fortrea

Clinical Project Manager II

Durham, NC · On-site

Our FSO team is seeking an Cell & Gene Therapy Clinical Project Manager to join our growing team ... to the contract. Project Managers will work to develop and lead high performing teams by ...

Emerus

Ensure that all required contracts are in place * Report on project budgets * Provide frequent ... Develop and manage Activation and Operations Readiness plans for new hospital openings * Lead end ...

Emerus

Clinical Project Manager

Ensure that all required contracts are in place * Report on project budgets * Provide frequent ... Develop and manage Activation and Operations Readiness plans for new hospital openings * Lead end ...

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How much do contract clinical project manager jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for contract 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 are the key skills and qualifications needed to thrive in the Contract Clinical Project Manager position, and why are they important?

To thrive as a Contract Clinical Project Manager, you need a solid background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), GCP guidelines, and certifications such as PMP or CCRA are highly valued. Exceptional organizational, leadership, and cross-functional communication skills help manage timelines, stakeholders, and remote project teams effectively. These competencies ensure studies are delivered on schedule, within budget, and in accordance with regulatory standards.

What are the typical challenges faced by Contract Clinical Project Managers, and how can they be addressed?

Contract Clinical Project Managers often navigate challenges such as balancing tight project timelines, ensuring compliance across multiple sites, and managing cross-functional teams with varying priorities. Adaptability and strong organizational skills are crucial for quickly resolving issues, reallocating resources, and maintaining clear communication between sponsors, CROs, and site staff. Proactive risk management, regular status reporting, and agile project adjustments can significantly streamline workflow and mitigate setbacks. By building collaborative relationships and fostering open communication, project managers can more efficiently address emerging challenges and keep clinical trials on track.

What is a Contract Clinical Project Manager job?

A Contract Clinical Project Manager oversees the planning, execution, and completion of clinical trials on a contract basis, typically for pharmaceutical or biotech companies. They ensure studies adhere to regulatory requirements, timelines, and budgets while coordinating cross-functional teams. Unlike permanent roles, contract positions are temporary and project-specific, offering flexibility and diverse experience across multiple organizations.

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Contract Clinical Project Manager jobs near you
Infographic showing various Contract Clinical Project Manager job openings in the United States as of July 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.

Clinical Project Manager/ Sr Project Manager

Theradex Oncology

Princeton, NJ • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago

Job description

Who We Are
Celebrating 40+ years!
Theradex Oncology is a full-service CRO specializing in oncology. The company manages global oncology trials and programs. The company was founded in 1982 working with the National Cancer Institute, which led to its expansion to working with industry sponsors developing cancer therapeutics. As a service-based company we support both domestic and international sponsors in the conduct of both early and late phase trials.
What You'll Do
As part of Theradex Oncology, you will have the opportunity to work with one of the largest professional teams focused solely on the development of cancer therapies. Cancer research continues to evolve as new therapies and therapeutic approaches are discovered, as part of the team you will work to support our sponsors in the development of these therapies. Theradex Oncology is an environment for highly motivated individuals who want to make a difference.
Opportunity
Clinical Project Manager or Sr Clinical Project Manager based on experience.
Location: USA Remote
Theradex Project Managers oversee global phase I - III oncology clinical trials from feasibility and startup through closeout to ensure processes, timelines, contracts, ICH/GCP adherence and quality standards are met. As a key point of contact you'll interface directly with sponsors, vendors, cross-functional team members and investigative sites. You'll identify and evaluate risks, interpret data on complex issues and implement solutions to ensure successful completion of oncology trials.
Key responsibilities:
  • Clinical Project Leadership: Drive the successful execution and proactive management of clinical projects. Serve as the subject matter expert for assigned protocols and provide guidance to cross-functional study teams.
  • Study Oversight: Monitor study enrollment, retention, and metrics to identify trends and act on deviations. Develop and implement strategic solutions for recruitment and retention challenges. Ensure accurate study information is reflected in status reports and clinical trial platforms.
  • Risk and Quality Management: Proactively identify and communicate operational risks, aligning with the study team on mitigation strategies. Oversee the development and adherence to study-specific oversight and Corrective and Preventive Action (CAPA) plans.
  • Compliance and Audits: Manage the Trial Master File (TMF) for Clinical Operations documentation and ensure inspection readiness. Collaborate with Quality Assurance for internal and external audits.
  • Budget and Timelines: Proactively manage study-specific timelines and budgets. Review and approve invoices and timesheets. Identify and initiate Change Order (CO) activities as required to maintain project scope.
  • Team Management: Lead and manage the day-to-day activities of the study team, including leading team meetings and conducting study-specific training.

What You Need
Education and Experience:
  • BS. required- preferably in a life science field or equivalent (includes RN degree)
    MS. or PhD. preferred
  • Healthcare professional with at least 4 years of clinical experience, or Science Graduate with at least 4 years experience in clinical research, with a track record in successfully managing clinical trial sites
  • Prior project management experience required
  • High level of proficiency with Excel and MS Office; ability to master various electronic platforms for data entry and clinical trial management
  • Experience with oncology clinical trials and/or cancer therapies is highly preferred (required for senior level project managers)
  • Prior involvement with with CAR-T or other gene/cell therapies is highly preferred
  • Prior experience in a CRO/pharmaceutical environment preferred (required for senior level project managers)
  • Must be fluent in English (verbal and written)

Skills and Competencies
  • Well-developed critical thinking and analytical skills, with the ability to anticipate problems relating to projects and to develop and implement solutions
  • Able to seek out multiple and diverse perspectives; open to continuously refining your approach based on feedback and new information
  • Knowledgeable of the initiation, conduct, and completion of clinical trials, study endpoints, and clinical databases
  • Well-developed and effective written and verbal communication skills, including report writing, preparing, and delivering presentations, and various correspondence and meeting platforms
  • Effective knowledge of the drug development process
Additional Requirements
  • Ability to travel occasionally up to 30% when required, domestic and/or global
  • Valid Driver's License an advantage
  • Basic knowledge of one (or more) European language an advantage

What We Offer
At Theradex we offer a supportive culture that puts people first. Our employees are eligible to participate in our comprehensive benefits package which includes medical, dental and vision coverage; life insurance, disability insurance (STD/LTD), company matched 401(k), very competitive tuition reimbursement, generous vacation/sick plans, flexible work schedules, employee discounts and other company provided benefits. The annual base salary for this position ranges from $105,000-$165,000 with bonus potential. We will assess the specific title and level of entry during the interview and assessment process since the actual salary offer will be based on a number of factors, including but not limited to the candidate's qualifications, experience, skills, and competencies for the role.
This position is not eligible for company provided sponsorship or relocation.
Theradex is an Equal Opportunity Employer.

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