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Clinical Project Manager Jobs in Raleigh, NC (NOW HIRING)

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Clinical Project Manager information

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How much do clinical project manager jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical project manager in Raleigh, NC is $59.01, according to ZipRecruiter salary data. Most workers in this role earn between $41.11 and $69.18 per hour, depending on experience, location, and employer.

How much do clinical project managers earn?

Clinical project managers typically earn between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. Compensation may also include bonuses and benefits related to project scope and complexity.

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 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 are the most commonly searched types of Clinical Project jobs in Raleigh, NC? The most popular types of Clinical Project jobs in Raleigh, NC are:
What are popular job titles related to Clinical Project Manager jobs in Raleigh, NC? For Clinical Project Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What cities near Raleigh, NC are hiring for Clinical Project Manager jobs? Cities near Raleigh, NC with the most Clinical Project Manager job openings:
Infographic showing various Clinical Project Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 84% Full Time, 12% Part Time, and 4% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $122,736 per year, or $59 per hour.

Senior Clinical Project Manager, Phase I

Fortrea

Durham, NC • On-site

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 12 days ago


Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

25th of 73 rated research


Job description

Our Phase I team is seeking a Sr. Clinical Project Manager to join our growing team. This role requires 4-5+ years of global project management experience, with mandatory experience in phase I. Candidates must be based in the United States or Canada.

Job Overview:

At times working under the direction of a Project Director, the Senior Project Manager oversees and manages domestic, regional and/or global projects. Responsibilities typically include developing and managing project teams, communications, risk, scope, schedule, cost, quality, and stakeholders, effectively ensuring that variance from plan is proactively and effectively mitigated and client expectations are met. The Senior Project Manager is expected to have a working knowledge of drug development and clinical trial execution. They also compile and drive documentation for the project, ensuring the accuracy and quality of regulatory data. The Senior Project Manager may also have line management and / or business development responsibilities.

    Summary of Responsibilities:

    • Operational delivery.
    • Accountable for project delivery with regards to agreed time, scope, cost, and quality.
    • TEAM COMMUNICATION: Serve as key client contact for assigned projects, establishing working relationships with client project teams which result in client satisfaction, operational excellence and thereby increase potential for repeat business.
    • Lead core project team(s) and facilitate team's ability to lead extended project team(s), ensuring effective cross-functional teamwork among project team members including both internal and external stakeholders. Depending on size and scope of project(s), this job duty may be performed in collaboration with a Project Director.
    • Serve as escalation point for project issues to internal and external stakeholders, as appropriate.
    • TEAM COMMUNICATION: Proactively identify and resolve conflicts as needed.
    • COST: Understand the project delivery strategy, costing assumptions and resulting budget for assigned project(s).
    • SCOPE: Deliver project(s) to scope, schedule, and costs, ensuring all remain on track with the contract and with financial performance targets. Initiate and implement appropriate actions to proactively manage the change control process both internally and externally.
    • RISK: Proactively lead both quality control and risk assurance activities to ensure project deliverables are met according to regulatory, Fortrea and client requirements.
    • QUALITY: Create and manage variance to required project plans. Per SOPs, implement and monitor progress against project plans and revise, as necessary. Ensure that all staff allocated to assigned project(s) adheres to professional standards and SOPs, providing performance feedback to team member's respective supervisors.
    • Aid in development and maintenance of key project performance indicators for client specified metrics, ensuring that the KPIs are within scope of the project contract.
    • Define and manage project resource needs and establish succession plans for key resources.
    • Business Development.
    • In collaboration with relevant departments, prepare and deliver presentations for new business as required.
    • Perform other duties as assigned by management.
    • Line Management and Talent Development.
    • Trains and mentors PM Academy PCs in multiple areas of expertise.
    • May be responsible for Line Management and Talent Development.
    • Ensures allocated resources are aligned with current and forecasted work in terms of capability, quantity, timing, and efficiency.
    • May be responsible for on-boarding, development, and retention of high performing talent; strengthening and deepening talent bench and succession.
    • Assesses project management competencies for assigned staff in order to create developmental plans that will increase competencies and close performance gaps.
    • Provides line management and technical support to assigned project leaders, including training, development, and performance review of assigned staff.
    • 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 seven (7) years of relevant clinical research experience in a pharmaceutical company/CRO, including at least two (2) years of full project management responsibility.
    • Phase I experience
    • 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.
    • Good knowledge of project management processes.
    • 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
    • Biotech experience
    • Fluent in Chinese/Mandarin

    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): $140-150k

    #LI - Remote

    Applications will be accepted on an ongoing basis.

    Work Environment:

    • Work is performed in an office environment with exposure to electrical office equipment.

    • 30% travel

    Physical Requirements:

    • Ability to sit for extended periods and operate a vehicle safely.

    • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.

    • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.

    • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

    • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

    • Regular and consistent attendance.

    • Varied hours may be required.

    Learn more about our EEO & Accommodations request here.


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