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Clinical Project Manager

Blue Bell, PA · Remote

Your focus will be on coordinating clinical project and program management delivery, resolving issues, and developing team capability. This role will align under the Biotech (IBT) division. Key ...

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Clinical Project Manager

Blue Bell, PA · On-site

Your focus will be on coordinating clinical project and program management delivery, resolving issues, and developing team capability. This role will align under the Biotech (IBT) division. Key ...

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Clinical Project Manager III

Bedford, MA

Responsible for insuring clinical project risks, both technical risks and management risks, are identified and appropriate risk mitigation plans are developed and executed. Track and respond to risk ...

Werfen

Clinical Project Manager III

Bedford, MA · On-site

Responsible for insuring clinical project risks, both technical risks and management risks, are identified and appropriate risk mitigation plans are developed and executed. Track and respond to risk ...

Werfen

Clinical Project Manager III

Bedford, MA · On-site

Responsible for insuring clinical project risks, both technical risks and management risks, are identified and appropriate risk mitigation plans are developed and executed. Track and respond to risk ...

Werfen

Clinical Project Manager III

Bedford, MA

Responsible for insuring clinical project risks, both technical risks and management risks, are identified and appropriate risk mitigation plans are developed and executed. Track and respond to risk ...

Werfen

Clinical Project Manager III

Bedford, MA

Responsible for insuring clinical project risks, both technical risks and management risks, are identified and appropriate risk mitigation plans are developed and executed. Track and respond to risk ...

Sigmaways Inc

Clinical Project Manager II/III

Tucson, AZ · On-site

... Clinical Operations Biometrics (COBM) Leadership Team, Life Cycle Teams (LCTs) and Life Cycle ... Applies project management skills and experience in delivering projects on time, within budget and ...

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How much do clinical project management jobs pay per hour?

As of Jun 1, 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 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 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 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 degree do you need to be a clinical project manager?

A clinical project manager typically needs at least a bachelor's degree in a health-related field such as life sciences, nursing, or healthcare administration. Many employers prefer candidates with a master's degree or relevant certifications like PMP (Project Management Professional) to demonstrate project management skills and industry knowledge.

What is the highest paid project manager?

In clinical project management, the highest paid professionals are often senior or program managers with extensive experience, specialized skills, and certifications like PMP or PMI-ACP. Salaries can exceed $150,000 annually, especially in the pharmaceutical or biotech industries, and may include bonuses and other incentives based on project scope and complexity.

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.

More about Clinical Project Management jobs
What cities are hiring for Clinical Project Management jobs? Cities with the most Clinical Project Management job openings:
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Clinical Project Management jobs near you
Infographic showing various Clinical Project Management job openings in the United States as of May 2026, with employment types broken down into 92% Full Time, 6% Part Time, and 2% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.
Associate Director, Clinical Project Management

Associate Director, Clinical Project Management

Crinetics Pharmaceuticals

Remote

$158K - $197K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 18 days ago

Job description

Position Summary:
The Associate Director, Clinical Project Management is responsible for oversight of Clinical Project Management activities for multiple studies and molecules, including timeline, risk, and budget management for all clinical trials managed by Clinical Operations.
Essential Job Functions and Responsibilities:
These may include but are not limited to:
  • Oversee timeline, budget and accruals for the clinical studies and clinical programs within the Clinical Operations group.
  • Develop, maintain, and manage high-quality consistent study processes and templates with cross-functional Clinical Operations peers to drive consistent and reliable clinical study outcomes.
  • In collaboration with the Project and Portfolio Management, provide clinical program timeline and budget estimates to support annual budgets and long-range planning (LRP).
  • Oversee and mentor team of Clinical Project Managers as needed.
  • Develop and oversee policies and procedures aimed to streamline Clinical Project Management process.
  • In collaboration with Clinical Trial Operations and Project and Portfolio Management, provide input on annual planning activities to meet corporate study and program objectives.
  • Subject Matter Expert (SME) for study and program clinical timelines and budgets.
  • Oversee routine status reporting including study timeline and budget dashboards and management updates.
  • Ensure teams are providing monthly milestone and timeline updates to Project and Portfolio Management for entry into corporate project management system.
  • In collaboration with Project and Portfolio Management, develop program scenario plans and support life cycle management activities as needed, support creation and incorporation of resource demand algorithms into project management software.
  • Oversee and streamline monthly accrual process in partnership with finance.
  • Facilitate and oversee cost accruals by study managers to ensure accuracy.
  • Meet with finance periodically to review accrued costs against forecasts and troubleshoot variances, and to oversee overall spend for studies & programs.
  • Identify potential budget issues and recommend and implement solutions or corrective actions as needed.
  • Provide program-level timeline and financial health summaries for management periodically
  • Other duties as assigned.

Education and Experience:
Required:
  • Bachelor's degree in a related discipline required; a combination of relevant education and applicable job experience may be considered.
  • Minimum of 10 years of progressive experience in clinical project management within a CRO, biotechnology, or pharmaceutical organization, including people leadership responsibilities
  • 7 years of supervisory experience.
  • Strong understanding of drug development, clinical operations, and clinical financial management.
  • Demonstrated leadership capability with experience mentoring and overseeing project management staff.
  • Excellent organizational, time management, and communication skills, with the ability to manage multiple priorities in a matrix environment.

Physical Demands and Work Environment:
Physical Activities: On a continuous basis, sit at a desk for extended periods of time; intermittently answer telephone calls and use a keyboard to communicate through written means. Some walking and lifting up to 25 lbs. may be required. The noise level in the work environment is typically low to moderate. The physical demands described above are representative of those that must be met by an employee to successfully perform the essential functions and responsibilities of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions and responsibilities.
Laboratory Activities (if applicable): Biology and chemical laboratory environment experience needed. Environmental health and safety requirements also apply.
Travel:
You may be required to travel for up to 5% of your time.
Equal Opportunity Employer:
Crinetics is proud to be an Equal Opportunity Employer. We provide equal employment opportunities to all employees and applicants without regard to sex, sexual orientation, gender identity or expression, pregnancy, race, color, creed, national or ethnic origin, citizenship status, religion, disability, marital or civil union status, age, genetic information, veteran status, or any other characteristic protected by applicable law.
Salary Range
The salary range for this position is: $158,000 - $197,000.
In addition to your base pay, our total rewards program consists of a discretionary annual target bonus, stock options, ESPP, and 401k match. We also provide top-notch health insurance plans for employees (and their families) to include medical, dental, vision and basic life insurance, 20 days of PTO, 10 paid holidays, and a winter company shutdown.

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