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

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

Leading the global study team with full accountability for study deliverables regarding quality ... Overseeing projects to ensure completion on-time, within scope, and budget; tracking project ...

Leading the global study team with full accountability for study deliverables regarding quality ... Overseeing projects to ensure completion on-time, within scope, and budget; tracking project ...

Clinical Project Manager- IVD

Durham, NC · On-site

$93K - $232K/yr

Leading the global study team with full accountability for study deliverables regarding quality ... Overseeing projects to ensure completion on-time, within scope, and budget; tracking project ...

Clinical Program Manager

Durham, NC · On-site

$93K - $285K/yr

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.

Clinical Program Manager

Durham, NC · On-site

$93K - $285K/yr

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.

Showing results 21-40

Clinical Project Leader information

See Raleigh, NC salary details

$32

$61

$79

How much do clinical project leader jobs pay per hour?

As of Sep 6, 2026, the average hourly pay for clinical project leader in Raleigh, NC is $61.24, according to ZipRecruiter salary data. Most workers in this role earn between $49.52 and $76.39 per hour, depending on experience, location, and employer.

What is a clinical project leader?

Clinical Project Leaders are professionals responsible for overseeing and managing clinical trials and research projects within the pharmaceutical, biotechnology, or medical device industries. They coordinate study teams, ensure regulatory compliance, manage timelines and budgets, and serve as the main point of contact between sponsors, investigators, and regulatory bodies. Their role is essential in ensuring that clinical studies are conducted efficiently, ethically, and in accordance with all protocols and regulations.

What are the key skills and qualifications needed to thrive as a clinical project leader?

To thrive as a Clinical Project Leader, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a relevant degree and experience in the pharmaceutical or clinical trials industry. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and project management certifications like PMP are highly valuable. Exceptional leadership, problem-solving, and communication skills help drive team performance and stakeholder engagement. These competencies are essential to ensure that clinical projects are completed efficiently, compliantly, and to the highest quality standards.

What are some common challenges clinical project leaders face when managing multi-site clinical trials?

Clinical Project Leaders often encounter challenges related to coordinating activities across various trial sites, ensuring regulatory compliance, and maintaining consistent communication among cross-functional teams. Overseeing timelines and budgets while adapting to unforeseen issues, such as patient recruitment delays or protocol amendments, requires strong organizational and problem-solving skills. Effective collaboration with clinical research associates, data managers, and investigators is essential for overcoming these obstacles and ensuring the trial's success.

What does a clinical project leader do?

A clinical project leader oversees the planning, execution, and management of clinical trials to ensure they are completed on time, within scope, and budget. They coordinate with cross-functional teams, monitor progress, ensure compliance with regulatory standards, and utilize project management tools to deliver high-quality results.

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

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

Infographic showing various Clinical Project Leader job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 14% Part Time, and 4% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $127,379 per year, or $61.2 per hour.

Local Trial Manager (Sponsor Dedicated)

IQVIA, Inc.

Durham, NC • On-site

Full-time

Re-posted 9 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 226 rated it services


Job description

Internal Job Description
Job Overview
Associate Project Leads (Local Trial Managers) are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Associate Project Lead is a member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Clinical Project Management is focused on project delivery, productivity and quality resulting in strong financial performance and customer satisfaction. The Associate Project Lead support the efforts of CPM to drive operational excellence and strategic leadership with our customers. Associate Project Leads may run their own studies, as part of their development.
Essential Functions
• Provide input in to the development of integrated study management plans with the core project team and/or sub-team.
• Accountable for assigned portion of clinical studies as per the contract while optimizing speed, quality and cost of delivery and ensuring consistent use of study tools and training materials and compliance with standard processes, policies and procedures.
• Set objectives of project sub-team(s), according to agreed upon contract, strategy and approach, effectively communicate and assess performance.
• Collaborate with other functional groups within the company where necessary to support milestone achievement and to manage study issues and obstacles.
• Monitor progress against contract and prepare/present project and/or sub-team information proactively to internal stakeholders. Support the project leader to prepare/present project and/or sub-team information proactively to external stakeholders.
• Identify risk (positive and negative) and contingencies and partner with project leader in problem solving and resolution efforts.
• Achieve project quality by identifying quality risks and issues, responding to issues raised by project sub-team members and partner with project leader planning/implementing appropriate corrective and preventative action plans.
• May serve as primary (for small projects) or back-up project contact with customer.
• Lead the efforts of a project sub-team, responsible for managing cross-collaboration of the sub-team to support milestone achievement and to manage issues and obstacles.
• Support the project leader in ensuring the financial success of the project.
• Forecast and identify opportunities to accelerate activities to bring revenue forward in partnership with the senior project leader.
• Identify changes in scope and partner with project leader to manage change control process as necessary.
• Identify lessons learned and implement best practices.
• May be assigned as the primary contact for vendors leading project vendor management and vendor management related activities as per project requirements
Qualifications
• Bachelor's Degree In life sciences or related field required Req
• 2 years clinical research experience in project management or trial management
• Requires intermediate level knowledge of principles, theories, and concepts of a job area, typically obtained through advanced education combined with experience.
• Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying applicable clinical research regulatory requirements i.e. ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial conduct. Broad protocol knowledge, therapeutic knowledge desired.;
• Communication - Strong written and verbal communication skills including good command of English language. Strong presentation skills.
• Problem solving - Strong problem solving skills.
• Organization - Planning, time management and prioritization skills. Ability to organize resources needed to accomplish tasks, set objectives and provide clear direction to others, experience planning activities in advance and taking account of possible changing circumstances.
• Prioritization - Ability to handle conflicting priorities.
• Quality - Attention to detail and accuracy in work. Results-oriented approach to work towards delivery and output.
• IT Skills - Good software and computer skills, including MS Office applications including but not limited to Microsoft Word, Excel and PowerPoint.
• Collaboration - Ability to establish and maintain effective working relationships with coworkers, managers and clients. Strong customer service skills.
• Cross-collaboration - Ability to work across geographies displaying high awareness and understanding of cultural differences.
• Finances - Good understanding of project financials.
• IQVIA Core Competencies - Ability to demonstrate all IQVIA competencies (Client Focus, Collaboration, Communication, innovation, Ownership).
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 at https://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 $68,400.00 - $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