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Clinical Trials Project Manager Jobs (NOW HIRING)

Tango Therapeutics

Clinical Trials Manager

Boston, MA · On-site

... complex clinical trials under CTL leadership. In addition, CTM will be responsible for site ... Strong vendor management and project management skills * Leadership skills with the ability to lead ...

Socket.dev

Clinical Trials Manager

Boston, MA · On-site

... complex clinical trials under CTL leadership. In addition, CTM will be responsible for site ... Strong vendor management and project management skills * Leadership skills with the ability to lead ...

Worldwide Clinical Trials Holdings, Inc.

NY · On-site

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... What the Project Manager does at Worldwide The Project Manager (PM) will manage one or more ...

LabConnect

Manager, Project Management

Johnson City, TN · On-site +1

The Manager of Project Management assigns clinical trials study management responsibilities to a designated Project Manager, along with performing duties as project manager on their own assigned ...

Gilead

Clinical Trials Manager

Foster City, CA · On-site

You may also participate in strategic initiatives / projects. Job Responsibilities: * Manages a ... support clinical trials. * May be required to present at internal or external meetings (i.e ...

labconnect

Manager, Project Management

The Manager of Project Management assigns clinical trials study management responsibilities to a designated Project Manager, along with performing duties as project manager on their own assigned ...

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

As of Sep 11, 2026, the average hourly pay for clinical trials 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 does a clinical trials project manager do?

A Clinical Trials Project Manager oversees the planning, execution, and completion of clinical research studies. They coordinate teams, manage timelines and budgets, ensure regulatory compliance, and communicate with stakeholders such as sponsors and regulatory agencies. Their role is crucial in ensuring that clinical trials run smoothly, meet all quality standards, and produce reliable data for new medical treatments or drugs.

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

To thrive as a Clinical Trials Project Manager, you need a strong background in life sciences, clinical research experience, and often a relevant degree or certification such as a PMP or ACRP credential. Familiarity with clinical trial management systems (CTMS), regulatory compliance standards like GCP, and project management tools is essential. Excellent organizational, leadership, and communication skills help coordinate cross-functional teams and manage complex timelines. These skills ensure trials are conducted efficiently, compliantly, and safely, supporting successful study outcomes.

What are the most common challenges faced by clinical trials project managers and how can they be addressed?

Clinical Trials Project Managers often encounter challenges such as managing complex timelines, ensuring regulatory compliance across multiple sites, and coordinating communication among diverse stakeholders. To address these, it is important to establish clear project plans, foster open communication channels with site teams and sponsors, and stay updated on regulatory requirements. Utilizing project management tools and regularly scheduled meetings can also help ensure that tasks are on track and potential issues are identified early.

What is the difference between Clinical Trials Project Manager vs Clinical Research Coordinator?

AspectClinical Trials Project ManagerClinical Research Coordinator
CredentialsBachelor's degree, often with project management certificationBachelor's degree in health sciences or related field
Work EnvironmentOversees multiple trials, manages teams, and coordinates with sponsorsHandles daily trial activities at clinical sites, interacts directly with participants
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical sites
Search & Comparison IntentFocuses on project management in clinical trialsFocuses on site-level trial coordination

The Clinical Trials Project Manager primarily oversees multiple clinical trials, managing teams and ensuring project milestones are met. In contrast, the Clinical Research Coordinator handles the day-to-day activities at clinical sites, working directly with participants. Both roles require relevant healthcare or research credentials but differ in scope and responsibilities within the clinical research process.

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Clinical Trials Project Manager jobs near you
Infographic showing various Clinical Trials Project Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.

Clinical Trials Manager

Foster City, CA • On-site

Integrated Resources INC
Recruiting and Staffing Services • 51 - 200 employees
Learn more about Integrated Resources INCexternal

Contractor

Re-posted 26 days ago

Job description

Company Description

Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.

Job Description

Job Description:

  • In partnership with CPMs, provides guidance and daily oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines.
  • Coaches members of a work team and ensures adherence to established guidelines.
  • Provide input to program budget and timelines to ensure successful management of all aspects of international clinical trials.
  • Anticipates obstacles and client difficulties and implements solutions to achieve project goals.
  • Must meet all requirements for Principal Clinical Research Associate position and have demonstrated proficiency in all relevant areas.
  • Assists CPM in revising project timelines/budgets as necessary.
  • Works with management on departmental issues, providing input to clinical operations strategies and work plans.
  • Communicates with functional peers regarding project status and issues and ensure project team goals are met.
  • Contributes to development of abstracts, presentations and manuscripts.
  • Participate in the recruiting and hiring process for CPA/CRAs and support their professional development.
  • Participate in training of CPAs and CRAs.
  • Provide guidance and training to CROs, vendors, investigators, and study coordinators on study requirements.
  • Excellent interpersonal skills and demonstrated ability to lead is required.
  • Must be able to resolve problems using national and international regulations, guidelines, and investigator interaction.
  • Strong communication and influence skills and ability to create a clear sense of direction is necessary.
  • Must be able to resolve problems using national and international regulations, guidelines, and investigator interaction.
  • Must have a demonstrated ability to successfully develop, implement, and manage Clinical Trials.
Additional Information

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus.

Thank you.


Kind Regards,

Harris Kaushik

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - (650)-399-0891

Gold Seal JCAHO Certified for Health Care Staffing

"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)

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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996

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