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Contract Clinical Project Manager Jobs in Raleigh, NC

IQVIA

Sr. Clinical Project Manager, IQVIA Biotech

Durham, NC · On-site

$93K - $232K/yr

IQVIA Biotech is seeking a Sr. Clinical Project Manager with experience in the following therapeutics: Cardiovascular, Renal, and Metabolic. IQVIA Biotech is a full-service CRO purpose-built to serve ...

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IQVIA

Senior Clinical Project Manager, CNS

Durham, NC · On-site

$93K - $232K/yr

We are seeking a US-based Senior Project Manager with proven experience in Central Nervous System (CNS) clinical trials to join IQVIA Biotech. This role is ideal for a seasoned project management ...

Fortrea

Clinical Team Lead, FSP - Oncology

Durham, NC · Remote

CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinical ...

Fortrea

Clinical Team Lead, FSP - Oncology

Durham, NC · Remote

CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinical ...

IQVIA, Inc.

Senior Clinical Lead- CNS

Durham, NC · On-site

Our Senior Clinical Leads oversee our Clinical Trial Management teams. In support of the Project ... Monitor clinical progress against contract and prepare/present project information proactively to ...

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

As of Jun 17, 2026, the average hourly pay for contract clinical project manager in Raleigh, NC is $59.00, 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 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.

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:
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Contract Clinical Project Manager jobs near you
Sr. Clinical Project Manager, IQVIA Biotech

Sr. Clinical Project Manager, IQVIA Biotech

IQVIA

Durham, NC • On-site

$93K - $232K/yr

Full-time

Posted yesterday

IQVIA rating

8.2

Company rating: 8.2 out of 10

Based on 52 frontline employees who took The Breakroom Quiz

46th of 204 rated it services

Job description

IQVIA Biotech is seeking a Sr. Clinical Project Manager with experience in the following therapeutics: Cardiovascular, Renal, and Metabolic.

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.

Overview
The Senior Clinical Project Manager is a key leader in the delivery of clinical trials, partnering with cross-functional teams and clients to accelerate the development of life-changing therapies. This role is responsible for end-to-end clinical study execution, ensuring projects are delivered on time, within scope, and on budget, while maintaining the highest standards of quality and compliance. The Senior Clinical Project Manager provides strategic oversight, operational leadership, and serves as the primary point of contact for sponsors.

Key Responsibilities

  • Lead the planning, execution, and delivery of medium to large, multi-regional clinical studies in alignment with contractual requirements, SOPs, and regulatory standards.
  • Develop and implement integrated study management plans, ensuring consistency in processes, tools, and training.
  • Serve as the primary liaison with sponsors, building strong client relationships and ensuring transparent communication on project status, risks, and deliverables.
  • Set direction and objectives for cross-functional project teams; monitor performance and drive accountability to meet milestones.
  • Partner with Business Development on bid defenses and contribute to winning new business, including leading presentations when applicable.
  • Proactively identify, assess, and mitigate risks; lead issue resolution and implement corrective and preventative action plans.
  • Collaborate with internal functional groups to support study execution and overcome operational challenges.
  • Monitor project progress against timelines, budget, and quality metrics; provide regular updates to internal and external stakeholders.
  • Ensure financial performance by managing budgets, forecasting revenue, and identifying opportunities to accelerate delivery.
  • Manage scope changes and oversee change control processes in collaboration with stakeholders.
  • Promote continuous improvement by sharing lessons learned and best practices.
  • Mentor and support the development of junior team members and contribute feedback on team performance.

Qualifications

  • Bachelor's Degree in Life Sciences or a related field required; advanced degree preferred.
  • Requires greater than 7 years of clinical research experience, including at least 4 years of project management experience, or an equivalent combination of education, training, and experience.
  • Proven ability to manage complex, global clinical trials and cross-functional teams.
  • Strong leadership, communication, and stakeholder management skills.
  • Demonstrated ability to manage budgets, timelines, and risk proactively.
  • Experience leading bid defenses and client engagements is preferred.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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