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Contract Clinical Project Manager Jobs (NOW HIRING)

Ipsen

Clinical Project Manager

Cambridge, MA · On-site

Clinical Project Manager Company: Ipsen Biopharmaceuticals Inc. About Ipsen: Ipsen is a mid-sized global biopharmaceutical company with a focus on transformative medicines in three therapeutic areas:

Collabera

Clinical Project Manager

North Chicago, IL · On-site

... Clinical Teams, and Public Affairs). Applies knowledge across multiple therapeutic areas to support ... Appropriately advises management of project risks and presents recommendations for resolution.

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

As of Jul 15, 2026, the average hourly pay for contract clinical project manager in the United States is $60.70, according to ZipRecruiter salary data. Most workers in this role earn between $42.31 and $71.15 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.

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Contract Clinical Project Manager jobs near you
Infographic showing various Contract Clinical Project Manager job openings in the United States as of July 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.
Clinical Project Manager, Sponsor Dedicated

Clinical Project Manager, Sponsor Dedicated

IQVIA, Inc.

Parsippany, NJ • On-site

Full-time

Posted 8 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

56th of 210 rated it services

Job description

*Home-based position - To be eligible for this position, you must reside in the same country where the job is located.
Position Specifics
This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout. Operating in a fast-paced environment with evolving priorities, the role ensures high-quality data delivery and regulatory compliance across all phases of the trial.
Candidates who will thrive in this role have expertise in drafting and managing informed consent process, managing site selection, patient recruitment strategies, and monitoring visit reports, while driving risk-based mitigation plans to proactively address study challenges. The position collaborates closely with cross-functional teams to support trial execution, maintain inspection readiness, and uphold GCP, SOP, and local regulatory standards.
Three years of clinical trial management experience is required within a role that is accountable for driving and owning local trial activities at the regional level.
Additional Information
Associate Clinical Project Managers (aCPM)/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 aCPM 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 aCPM supports the efforts of CPM to drive operational excellence and strategic leadership with our customers.
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.
  • Strong site engagement qualifications - able to interact with and drive change to address out of compliance sites.
  • 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.
  • Work with monitors to address systemic site issues.
  • 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
  • 3 years clinical trial management experience
  • 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 and ability to facilitate information sharing amongst stakeholders. Strong presentation skills.
  • Problem solving - Strong problem solving skills.
  • Proven ability to drive change management and follow through on changes to resolution
  • 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 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 $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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