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Clinical Project Manager Jobs (NOW HIRING)

Emerus

... project manager in healthcare, strongly preferred * Bachelor's Degree or higher required * PMP required * Clinical licensure or relevant clinical credential required (e.g. RN, LVN, ARRT, RRT/CRT ...

Emerus

Clinical Project Manager

... project manager in healthcare, strongly preferred * Bachelor's Degree or higher required * PMP required * Clinical licensure or relevant clinical credential required (e.g. RN, LVN, ARRT, RRT/CRT ...

IQVIA

RWE Clinical Project Manager (FSP)

Durham, NC · On-site

$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 ...

Collabera

Clinical Project Manager

North Chicago, IL

... 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 clinical project manager jobs pay per hour?

As of Aug 12, 2026, the average hourly pay for 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.

How much do clinical project managers earn?

Clinical project managers typically earn between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. Compensation may also include bonuses and benefits related to project scope and complexity.

What is the difference between Clinical Project Manager vs Clinical Research Associate?

AspectClinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMPUsually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors and sitesMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageFound in pharmaceutical, biotech, and CRO companies overseeing entire projectsPrimarily employed by CROs and sponsors to monitor trial sites

The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

What does a clinical project manager do?

A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.

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

To thrive as a Clinical Project Manager, you need expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.

What does a clinical project manager do?

A Clinical Project Manager oversees the planning, execution, and completion of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They coordinate teams, manage budgets, timelines, and ensure that studies comply with regulatory standards and company protocols. Clinical Project Managers act as the main point of contact between sponsors, vendors, and clinical research sites, working to ensure that trials progress smoothly and data integrity is maintained. Their role is critical in bringing new therapies and treatments to market safely and efficiently.

What are some common challenges clinical project managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.
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Clinical Project Manager jobs near you
Infographic showing various Clinical Project Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.

Clinical Project Manager

Relay Therapeutics

Cambridge, MA • On-site

Full-time

Re-posted 14 days ago

Job description

The Opportunity:
As Clinical Project Manager, you will be accountable for managing clinical studies that will lead the biopharma industry in speed and quality of clinical study design and execution. You will be an integral member of the Relay Tx scientific team, responsible for the execution of clinical studies that will translate Relay's innovative science into impactful medicines for patients.
The Role:
  • Contribute to the planning, implementation, and execution of a global clinical trial(s) from startup through closeout. Lead and manage integration of the project team activities, leveraging internal and development partner resources, expertise and knowledge, along with optimizing CRO resources, expertise and knowledge.
  • Collaborate and partner with a dynamic Relay cross-functional team to deliver clinical studies that are on time and within budget guidelines, while ensuring quality in accordance with the protocol and ICH GCP guidelines.
  • Provide leadership and input into global patient recruitment plans including the documentation of assumptions.
  • Develop and maintain strong working relationships with internal and external stakeholders (cross-functional team members, Contract Research Organizations (CROs), external experts, and clinical site staff), ensuring high-quality services are executed in a timely and cost-effective manner.
  • Manage reports for communicating study progress and key metrics to Senior Management and program teams.
  • Contribute to or author key study documents including, but not limited to, protocols, informed consent forms, case report forms, study governance committee charters (e.g., data monitoring committee), study plans and clinical study reports.
  • Accountable for effective vendor management by:
    • serving as primary point of contact for contracted CROs and vendors
    • identifying potential risks and proactively resolving issues with CROs and vendors
    • ensuring vendor contracts meet requirements and are efficiently executed with key performance indicators
    • partnering with the vendor to ensure accurate budgeting and accrual of costs throughout duration of each clinical study
  • Ensure reliable quality data is delivered by reviewing monitoring reports, protocol deviations, clinical data listings and performing or overseeing site monitoring visits, as needed.
  • Develops and drives granular clinical study timelines and enrollment projections and contributes to the development of Key Performance Metrics and risk mitigation strategies.
  • Monitor and manage vendor and site performance, trial progress and quality through evaluation of defined study performance metrics.
  • Proactively identify risks and issues, and work with the trial team to assess impact, devise strategies to implement corrective actions or preventive measures to mitigate risk.
  • Develop action plans to address protocol compliance, safety, data and administrative issues with clinical sites and CROs.
  • Lead coordination with CROs on site selection, IRB/EC submissions and queries, site initiation and close-out planning.
  • Provide oversight and ensure maintenance of clinical trial master files (TMF) to ensure compliance with required regulatory and ICH GCP quality standards and consistency with SOPs.
  • Plan, execute and lead study-specific meetings (internal study team meetings, vendor meetings, Investigator Meetings, etc.), as needed.
  • Support the preparation of regulatory filings (e.g. IND, NDA, orphan drug applications etc.) as needed.
  • Ensure inspection readiness by collaborating with CROs and providing support to clinical sites to prepare for and respond to audit/inspection findings conducted by internal QA and external regulatory agencies.
  • Obtains and maintains an in-depth understanding of the study protocol and related procedures to contribute strongly to Study Team knowledge by sharing best practices, making recommendations for continuous improvement, and training/mentoring as appropriate.
  • Fosters an environment of continuous improvement and actively participants in the recruitment, training and professional development of clinical operations team members

Your Background:
  • Minimum of 5-8 years of experience in clinical research with 1-2 years managing trials in the biotech/pharma industry. BA/BS preferably in a scientific or health-related discipline.
  • Experience managing global clinical trials and study teams across all stages (startup-closeout) of phase I-III studies and a strong working knowledge of GCP/ICH and other applicable regulations/guidelines required. Strong preference for tenured experience in the biotech/pharmaceutical industry in late phase clinical trials.
  • Solid experience and understanding of the challenges of navigating global study startup including the oversight of site startup processes and timelines.
  • Experience across several complex therapeutic areas. Oncology experience is a plus.
  • Solid understanding of the drug development process, ICH guidelines/GCP and specifically, each step within the clinical trial process.
  • Understand clinical study budgets, accruals, and forecasting with experience liaising with Finance as required.
  • Demonstrated ability to lead teams in a fast-paced matrixed environment, with the ability to manage and prioritize multiple tasks simultaneously.
  • Enjoy building relationships with CROs, KOLs and site personnel with a willingness to travel to establish and build relationships.
  • Experience in vendor selection and overseeing studies managed by a CRO.
  • Strong interpersonal and relationship-building skills; ability to influence and collaborate across functions and levels.
  • Demonstrated ability to problem solve and use clear judgment in relation to regulatory requirements, interactions with external parties, timelines, and complex clinical studies.
  • Independently motivated, detail oriented and good problem-solving ability (think outside of the box mentality).
  • Excellent oral and written communication, organizational and planning skills are required, with a proven ability to manage timelines and budget.
  • Detail-oriented, a self-starter and comfortable with broad responsibilities in an fast-paced, small company outsourced trial environment.

Estimated Salary Range: [$102,000 - $145,000].
The range provided above is based on what we believe to be a reasonable estimate for this job at the time of posting. Actual base salary will depend on a number of factors, including but not limited to, a candidate's education, experience, skills and location.
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About Relay Therapeutics
Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process with the goal of bringing life-changing therapies to patients. Built on unparalleled insights into protein motion and how this dynamic behavior relates to protein function, we aim to effectively drug protein targets that have previously been intractable, with an initial focus on enhancing small molecule therapeutic discovery in targeted oncology. Our Dynamo platform integrates an array of leading-edge experimental and computational approaches to provide a differentiated understanding of protein structure and motion to drug these targets. We have built a world-class team of leading experts from each of these disciplines, and they are driven by a deep collaboration at every step of our drug discovery process.
Our team is equal parts fearless and relentless, with a shared passion for working collaboratively in intellectually stimulating environments. If you're excited by the challenge of putting protein motion at the heart of drug discovery and passionate about making a difference in the lives of patients, join us!

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