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Clinical Project Management Jobs (NOW HIRING)

CTI

Clinical Project Coordinator

Raleigh, NC

Support Clinical Project Manager / Director in completing clinical project management activities; support activities throughout all phases of a clinical project, including any SOP-required ...

CTI

Clinical Project Coordinator

Raleigh, NC · On-site

Support Clinical Project Manager / Director in completing clinical project management activities; support activities throughout all phases of a clinical project, including any SOP-required ...

CTI

Clinical Project Coordinator

Covington, KY

Support Clinical Project Manager / Director in completing clinical project management activities; support activities throughout all phases of a clinical project, including any SOP-required ...

Pluto Health

Clinical Project Manager

Durham, NC · On-site

$85K - $120K/yr

As a Clinical Project Manager, you will play a critical role in leading cross-functional teams ... Utilize project management best practices to successfully execute projects, ensuring adherence to ...

ICON

Senior Clinical Project Manager

Blue Bell, PA · On-site

Extensive experience in global clinical project management, with a proven track record of leading successful projects in the pharmaceutical or biotech industry. * Strong proficiency in project ...

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Clinical Project Management information

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How much do clinical project management jobs pay per hour?

As of Aug 24, 2026, the average hourly pay for clinical project management 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 is clinical project management?

Clinical project management involves planning, coordinating, and overseeing clinical trials or research projects to ensure they are completed on time, within budget, and according to regulatory requirements. Clinical project managers are responsible for managing cross-functional teams, timelines, budgets, and resources, as well as communicating with stakeholders and ensuring compliance with Good Clinical Practice (GCP) guidelines. Their work is essential to the successful execution of clinical studies and the advancement of new medical treatments.

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

Clinical Project Managers often encounter challenges such as ensuring consistent protocol adherence across multiple sites, managing timelines with various stakeholders, and handling regulatory documentation for different regions. Communication is key, as PMs must keep both internal teams and external partners aligned despite geographic and cultural differences. Effective risk management and proactive problem-solving skills are essential to keep studies on track and maintain data quality.

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 a strong background in clinical research, project management, and regulatory compliance, often supported by a life sciences degree and relevant industry experience. Familiarity with clinical trial management systems (CTMS), GCP guidelines, and project management certifications like PMP are highly valued. Outstanding organizational, leadership, and communication skills help coordinate cross-functional teams and manage complex timelines. These competencies ensure clinical trials are conducted efficiently, compliantly, and within budget, ultimately supporting successful study outcomes.

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

AspectClinical Project ManagementClinical Research Associate
CredentialsTypically requires a degree in life sciences, project management certification (e.g., PMP)Usually holds a degree in life sciences or healthcare; certifications like CCRA are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates across departmentsMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageUsed by pharmaceutical, biotech companies, and CROs for overseeing projectsEmployed by sponsors, CROs, and sites to ensure trial quality and compliance

Clinical Project Managers focus on overseeing entire clinical trials, managing teams, and ensuring project milestones are met. Clinical Research Associates primarily monitor clinical sites and ensure compliance with protocols. Both roles are essential in the clinical research process but differ in scope and responsibilities.

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Clinical Project Management jobs near you
Infographic showing various Clinical Project Management job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, and 2% Contract. Highlights an 83% Physical, 2% Hybrid, and 15% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.

Supervisor, Clinical Project Management

Sharp Services

Bethlehem, PA • On-site

Full-time

Posted 18 days ago

Job description

At Sharp, being resourceful is a defining value, not just a buzzword. We adapt to changing circumstances; adjusting our plans when we need to. We think through how a project might play out so we can anticipate challenges while finding clever ways to solve problems.

We're looking for resourceful, adaptable professionals who can navigate evolving circumstances.

The Clinical Project Management, Team Leader will manage & mentor Clinical Project Managers & Project Coordinators. Clinical Team Leaders are responsible for overseeing all Clinical PM activities involved with the management of clinical supplies for assigned team & accounts. This includes but is not limited to the following services: procurement, distribution, formulation/development, manufacturing, packaging and analytical services. The Clinical Team Leader will be a project resource and escalation point for the Clinical Project Managers & Project Coordinators.


Essential Duties and Responsibilities

  • Direct line supervision of assigned Project Teams
  • Ensure training and development for Clinical Project Managers (PM), Project Coordinators (PC), Account Managers (AM)
  • Manage project coordination process and supporting framework for assigned PM/ PC team
  • Oversee PMs projects and timelines for adherence
  • Review incoming requests for assignments
  • Promote communication among team with leading regular meetings
  • Serve as the primary liaison for business partners
  • Interview business partner to obtain all relevant project information
  • Interpret protocols and protocol summaries and provide technical guidance to PM/PC team
  • Prepare project timeline with input from key operating departments and business partner
  • Ensure that Batch Records (BRs) are in compliance with cGMPs and SOPs in a timely, accurate and concise manner
  • Document and ensure that background information for all projects and maintain complete record files
  • Collaborate with key operating departments to meet internal dates for timely completion of requested activities
  • Work with colleagues to resolve potential conflicts with projects
  • Inform management and business partners of project delays and recommend appropriate solutions
  • Adhere to policies, processes and SOPs to ensure compliance with cGMP, FDA and any other regulatory regulations and standards


Qualifications:

  • Bachelors' Degree in the sciences and/or related experience
  • 5 years in experience in Project Management, preferably in pharmaceutical clinical supplies or clinical research/supply environment/ commercial packaging
  • Demonstrated ability to work independently, handle multiple tasks simultaneously and negotiate and meet critical timelines
  • Experience in managing people
  • Knowledge of cGMPs, FDA , DEA and OSHA Regulations and ISO guidelines, preferred
  • Basic knowledge of drug product nomenclature and drug development process

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