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Contract Clinical Project Manager Jobs in Raleigh, NC

CTI

Clinical Project Coordinator

Raleigh, NC · On-site

Support Clinical Project Manager / Director in completing clinical project management activities ... clinical contract research organization (CRO) focused on the advancement of treatments for ...

CTI

Clinical Project Coordinator

Raleigh, NC

Support Clinical Project Manager / Director in completing clinical project management activities ... clinical contract research organization (CRO) focused on the advancement of treatments for ...

Pluto Health

Clinical Project Manager

Durham, NC · On-site

$85K - $120K/yr

As a Clinical Project Manager, you will play a critical role in leading cross-functional teams, ensuring adherence to project timelines, budgets, and quality standards, while collaboratively working ...

IQVIA

Clinical Project Manager- Oncology

Durham, NC · On-site

Clinical Project Management is focused on project delivery, productivity and quality resulting in ... Monitor progress against contract and prepare/present project and/or sub-team information ...

IQVIA

Senior Clinical Project Manager

Durham, NC · On-site

Monitor progress against contract and prepare/present project information proactively to all ... clinical trial management experience. Experience in all aspects of clinical study planning and ...

IQVIA

Senior Clinical Project Manager

Durham, NC · On-site

Monitor progress against contract and prepare/present project information proactively to all ... clinical trial management experience. Experience in all aspects of clinical study planning and ...

IQVIA

Senior Clinical Project Manager- CNS

Durham, NC · On-site

Clinical Project Management is focused on project delivery, productivity and quality resulting in ... Monitor progress against contract and prepare/present project information proactively to all ...

IQVIA

RWE Clinical Project Manager

Durham, NC

$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 ...

IQVIA

Senior Clinical Project Manager- CNS

Durham, NC · On-site

Clinical Project Management is focused on project delivery, productivity and quality resulting in ... Monitor progress against contract and prepare/present project information proactively to all ...

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Contract Clinical Project Manager information

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

As of Aug 5, 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:
Contract Clinical Project Manager jobs near you
Infographic showing various Contract Clinical Project Manager job openings in Raleigh, NC as of July 2026, with employment types broken down into 2% As Needed, 74% Full Time, 17% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $122,736 per year, or $59 per hour.

Clinical Project Coordinator

CTI

Raleigh, NC • On-site

Full-time

Medical, PTO

Re-posted 17 days ago

Job description

Job Summary: The Clinical Project Coordinator position is responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, budgets and quality standards are being achieved. **Please note that this position is office based to be filled at our Covington, KY or Raleigh, NC office location.**
What You'll Do
  • Support Clinical Project Manager / Director in completing clinical project management activities; support activities throughout all phases of a clinical project, including any SOP-required deliverable as appropriate
  • Update Clinical Project Manager / Director on progress, outstanding items, and issues as they arise; support Clinical Project Manager / Director with issue resolution
  • Assist Clinical Project Manager / Director or Clinical Research Manager / Clinical Operations Director with preparing data reports for site and Clinical Research Associate (CRA) management; provide support for site management activities
  • Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in reviewing and maintaining these presentations and documents as required per CTI Standard Operating Procedures (SOPs)
  • Prepare initial drafts, including templates and content, of internal reports, external reports, newsletters, and other clinical project communications; distribute reports and communications to sites, vendors, Sponsors, and internal team members
  • Assist with tracking project scope and internal financial reporting
  • Prepare initial drafts of detailed meeting agendas and minutes; assist in initial review of meeting documents prepared by others; attend routine internal and external team meetings
  • Monitor and maintain tracking tools, clinical systems and shared document repositories utilized for clinical project management
  • Manage and maintain CTI clinical system user account requests
  • Support the review and tracking of site prescreening, screening, and enrollment activities as well as subject status information; follow up with internal clinical project team and/or sites as necessary regarding any identified issues
  • Support tracking of action items and internal team follow-up
  • Support and prepare / maintain tracking of clinical project start-up activities and milestones, including site selection and site start-up activities
  • Assist the clinical project team and/or the Feasibility Department with developing feasibility surveys and survey content; participate in feasibility calls; assist with any site follow-up needed throughout start-up
  • Assist clinical project team with tracking and filing of clinical project plan and/or Standard Operating Procedure (SOP)-related deviations
  • Support and maintain clinical project documents in paper and/or electronic Trial Master Files and support Clinical Project Manager / Director with TMF reconciliation and period review follow-up
  • Create and compile the Investigator Site File and Pharmacy Binde or Study Manual in collaboration with CPM/RASSU/Clinical Monitoring. Organize shipments to CRA/Site. Includes set-up and maintenance of Index with Comments.
  • Participate in preparing and following-up from internal and external audits; participate in audits as needed
  • Assist with the management of all clinical project-related supplies and drug management
  • Assist other departments as needed throughout all phases of clinical projects (e.g., Regulatory Affairs Study Start-up, Data Management, Safety, etc.)
  • Provide support in developing new Clinical Project Coordinators, Clinical Project Assistants, and Research Associates (RAs) in clinical projects
  • Assist with orientating new Clinical staff
  • Provide third party vendor support
  • Represent CTI in professional manner and foster collaboration with all clinical project teams / functional departments; assist in promoting interdepartmental cohesiveness

What You'll Bring
  • Bachelor's degree in allied health fields such as nursing, pharmacy, or health / natural science or an equivalent combination of education and relevant work experience
  • At least 1 year of experience in clinical research related field

About CTI
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com
Why CTI?
  • Advance Your Career - We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
  • Join an Award-Winning and Valued Team - We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
  • Make a Lasting Impact - We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.

Important NoteIn light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.
Please Note
  • We will never communicate with you via Microsoft Teams or text message
  • We will never ask for your bank account information at any point during the recruitment process

Equal Opportunity Employer/Veterans/Disabled
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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