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Clinical Trial Program Manager Jobs in Raleigh, NC

Clinical Program Manager

Durham, NC · On-site

$93K - $285K/yr

As Senior Project Leader/Clinical Program Manager you will liaise directly between IQVIA/sponsor functions and the customer, acting as that accountable point for delivery and quality whilst ...

Clinical Program Manager

Durham, NC · On-site

$93K - $285K/yr

As Senior Project Leader/Clinical Program Manager you will liaise directly between IQVIA/sponsor functions and the customer, acting as that accountable point for delivery and quality whilst ...

Clinical Program Manager

Durham, NC · On-site

$93K - $285K/yr

As Senior Project Leader/Clinical Program Manager you will liaise directly between IQVIA/sponsor functions and the customer, acting as that accountable point for delivery and quality whilst ...

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out ...

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out ...

Clinical Study Manager Location: Durham, North Carolina Type: 12-month Contract Work Model: Onsite ... Strong knowledge of clinical trial operations, study start-up, maintenance, and close-out ...

Senior Global Trial Manager

Durham, NC · On-site +1

$93K - $232K/yr

Ensuring clinical delivery of assigned projects in compliance with regulatory requirements ... We invest in integrated benefits programs and resources to take care of our employees' physical ...

Senior Global Trial Manager

Durham, NC · On-site +1

$93K - $232K/yr

Ensuring clinical delivery of assigned projects in compliance with regulatory requirements ... We invest in integrated benefits programs and resources to take care of our employees' physical ...

Senior Global Trial Manager

Durham, NC · On-site

$93K - $232K/yr

Ensuring clinical delivery of assigned projects in compliance with regulatory requirements ... We invest in integrated benefits programs and resources to take care of our employees' physical ...

Ensuring clinical delivery of assigned projects in compliance with regulatory requirements ... We invest in integrated benefits programs and resources to take care of our employees' physical ...

Lead end-to-end country-level trial management , from study start-up through database lock and closeout * Serve as the primary contact for assigned clinical trials within your country * Ensure ...

Remote (United States) Employment Type: Full-Time Our client is seeking a Budget Operations Specialist to support global clinical trial operations by managing investigator budgets, site setup, and ...

Showing results 41-60

Clinical Trial Program Manager information

See Raleigh, NC salary details

$28

$60

$93

How much do clinical trial program manager jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for clinical trial program manager in Raleigh, NC is $60.77, according to ZipRecruiter salary data. Most workers in this role earn between $49.33 and $68.46 per hour, depending on experience, location, and employer.

What does a clinical trial program manager do?

A Clinical Trial Program Manager oversees the planning, execution, and completion of clinical trials within an organization. They coordinate cross-functional teams, manage timelines and budgets, ensure compliance with regulatory guidelines, and maintain the quality and integrity of clinical data. Their role is essential for the successful development of new medical treatments, as they bridge communication between stakeholders, monitor progress, and address any issues that arise during trials.

What are some common challenges faced by clinical trial program managers, and how can they be addressed?

Clinical Trial Program Managers often encounter challenges such as managing complex timelines, coordinating multiple stakeholders, and ensuring regulatory compliance across different study sites. These challenges can be addressed by implementing robust project management tools, maintaining clear and consistent communication with cross-functional teams, and staying updated on regulatory requirements. Developing strong organizational skills and fostering collaborative relationships with investigators, sponsors, and regulatory bodies are also key to overcoming obstacles in this role.

What are the key skills and qualifications needed to thrive as a clinical trial program manager, and why are they important?

To thrive as a Clinical Trial Program Manager, you need strong project management skills, a background in life sciences or healthcare, and experience with clinical research regulations such as GCP, often supported by a relevant degree and certifications like PMP or ACRP. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and regulatory submission tools is typically required. Exceptional leadership, communication, and problem-solving abilities help you coordinate teams and manage complex stakeholder relationships. These skills ensure that clinical trials are conducted efficiently, compliantly, and successfully, leading to reliable study outcomes and regulatory approval.
What are popular job titles related to Clinical Trial Program Manager jobs in Raleigh, NC? For Clinical Trial Program Manager jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Clinical Trial Program Manager jobs in Raleigh, NC look for? The top searched job categories for Clinical Trial Program Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Clinical Trial Program Manager jobs? Cities near Raleigh, NC with the most Clinical Trial Program Manager job openings:
Infographic showing various Clinical Trial Program Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $126,404 per year, or $60.8 per hour.

Clinical Program Manager

IQVIA

Durham, NC • On-site

$93K - $285K/yr

Full-time

Posted 29 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

61st of 223 rated it services


Job description

Job Summary:

We are looking for Senior Project Leaders/Clinical Program Managers to join our innovative and dynamic group of global professionals dedicated to assisting our clients in driving healthcare forward. This is an important and high-profile role within our sponsor-dedicated business unit to enable medical breakthroughs that advance healthcare and patient treatment options around the world.

As Senior Project Leader/Clinical Program Manager you will liaise directly between IQVIA/sponsor functions and the customer, acting as that accountable point for delivery and quality whilst maintaining financial control. You will manage cross functional teams across this global organization and be supported by domain experts in every function, enabled by best-in-class technology and data analytics. This role owns study and or program level timelines and planning;
Microsoft Project (MSP) expertise is a must-have, as well as developed analytic skills.

Key collaborators are the Clinical Lead for site management, the Project Vendor Manager, the Project Management Analyst for project coordination, tracking and financial analysis, and the Site Activation Manager an expert in start-up.

IQVIA's size and global footprint will present you with the breadth of opportunities necessary to develop your career.

Typically assigned to one or two projects, or a program, responsibilities might include:

  • Leading global cross-functional project team delivery, accountable for achievement of milestones and quality of contracted scope
  • Serving as the primary contact with the customer for progress and governance
  • Developing study management plans and ensuring consistent use of study tools, training materials and compliance with standard processes, policies and procedures
  • Anticipating risk and implementing mitigation strategies
  • Managing study team assignments, accountability and resource requirements
  • Ensuring the study budget is managed proactively including scope changes and financial systems are accurate

Requirements:

  • Bachelors Degree
  • Professional Project Management certification is preferred
  • A minimum of 5 years' in Clinical Project Management in industry/CRO/business experience is required in clinical drug development
  • and/or clinical operations, clinical R&D experience preferred.
  • Prior experience leading a cross-functional global teams is required
  • Demonstrated ability to resolve conflict and influence teams without direct authority
  • Successful experience in planning and management of governance bodies is preferred
  • Proficient in MS Project is required

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 - $285,500.00. 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