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Contract Clinical Project Manager Jobs in Raleigh, NC

... project management experience. * Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas. IQVIA is a leading global provider of clinical ...

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

... project management experience. * Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas. IQVIA is a leading global provider of clinical ...

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

... project management experience. * Conceptual and practical knowledge of Product Development and basic knowledge of Clinical Operations or related areas. IQVIA is a leading global provider of clinical ...

CANDIDATE MUST BE CERTIFIED IN AT LEAST ONE CLINICAL APPLICATION The North Carolina Department of Health and Human Services requires the services of an EXPERT Epic Clinical project manager to manage ...

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 ...

Clinical Project Coordinator

Durham, NC · On-site

$51K - $127K/yr

IQVIA is looking for a Clinical Project Coordinator to join our growing team. Role can be homebased ... Manage study specific eTraining and oversee compliance. Support the updating and maintenance of ...

Clinical Project Coordinator

Durham, NC · On-site

$51K - $127K/yr

Support, with minimal supervision, the Project Leader (PL) and Clinical Project Manager (CPM) with project management activities to ensure all work is conducted in accordance with standard operating ...

Showing results 21-40

Contract Clinical Project Manager information

See Raleigh, NC salary details

$28

$59

$105

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

As of Aug 13, 2026, the average hourly pay for contract 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.

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?

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.

What are the most commonly searched types of Clinical Project Manager jobs in Raleigh, NC?

The most popular types of Clinical Project Manager jobs in Raleigh, NC are:

What are popular job titles related to Contract Clinical Project Manager jobs in Raleigh, NC?

For Contract Clinical Project Manager jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Contract Clinical Project Manager jobs in Raleigh, NC look for?

The top searched job categories for Contract Clinical Project Manager jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Contract Clinical Project Manager jobs?

Cities near Raleigh, NC with the most Contract Clinical Project Manager job openings:

Infographic showing various Contract Clinical Project Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Contract. Highlights an 100% In-person 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, Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 17 days ago


Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

26th 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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