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Clinical Trials Project Manager Jobs (NOW HIRING)

Worldwide Clinical Trials

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 ...

Worldwide

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ... What the Project Management department does at Worldwide**Worldwide Clinical Trials Project ...

Worldwide Clinical Trials

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 ...

Natera

Manager, Clinical Trials

OR · On-site +1

... project to ensure compliance and execution of project deliverables within the approved budget ... for clinical trials management expertise * Monitor and track clinical trial progress and provide ...

Worldwide

## Project Manager - Oncology - US/Canada - RemoteApplyremote type: Remotelocations: Virtual United ... We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers ...

Natera

Manager, Clinical Trials

$115K - $144K/yr

The Clinical Trial Manager should have experience in managing all aspects of the trials ... Ability to prioritize and handle multiple tasks and projects in a fast-paced environment The pay ...

Mount Sinai Medical Center

Description The Clinical Trials Manager coordinates and manages multiple clinical trials projects and protocols, including those from pharmaceutical companies. This individual instructs staff ...

WEP Clinical

Clinical Trial Project Manager

Lead the setup, execution, and close-out of clinical trials in compliance with WEP Clinical SOPs ... Manage project budgets, scope, and financial performance. * Oversee vendor performance and ...

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 ...

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Clinical Trials Project Manager information

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

As of Sep 10, 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.

Project Manager (US/CA)

Miami, FL • On-site, Remote

Worldwide Clinical Trials
Scientific Research and Development Services • 10K+ employees
Learn more about Worldwide Clinical Trialsexternal

Full-time

Posted 21 days ago

Job description

Who we are
We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.
Why Worldwide
We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us!
What the Project Manager does at Worldwide
The Project Manager (PM) will manage one or more allocated Phase I through IV Clinical Trials that may be local, regional or global in scope. WCT Project Managers are 100% accountable for the success of their projects.
Project Manager (PM) is responsible for the overall coordination and management of clinical trials from start up through close out activities.
Directs the technical, financial and operational aspects of the projects -- thus securing the successful completion of clinical trials.
Works with functional area leads to identify and evaluate fundamental project requirements, interpret data on complex issues, is responsible for contingency planning and implementation of rescue strategy where needed and ensure solutions are implemented.
Works to ensure that all project deliverables meet the customer's time/quality/cost expectations *
The PM, with support from the Project Management Directors, working in collaboration with other functional area leads, is accountable for ensuring that all project deliverables meet the customer/contract expectations.
What you will do
  • Lead core project team members and facilitate their ability to lead extended/complete project team
  • Lead cross unit coordination both internal and external, inclusive of sub-contractors
  • Define and manage project resource needs in conjunction with functional heads and establish contingency plans for key resources
  • Ensure successful design, implementation, tracking and revision of project plans for assigned projects
  • Promote effective teamwork among project team members; resolve conflicts as needed
  • Ensure appropriate communication on project-related matters with the PM Management

What you will bring to the role
  • Experience in managing projects in a multi-office environment
  • Demonstrated ability to handle multiple competing priorities; utilize resources effectively
  • Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system
  • Demonstrated ability to lead by example and to encourage team members to seek solutions
  • Excellent communication, planning and organizational skills
  • Self-motivated and excellent problem solving skills

Your experience
  • University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilities
  • Minimum of five (5) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks
  • In lieu of the above requirements, candidates with > five (5) years supervisory experience in a health care setting and four (4) years clinical research experience in the pharmaceutical or CRO industries will be considered and/or proven ability and demonstration of relevant experience and skills in clinical development
  • Thorough knowledge of project management processes
  • Thorough knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs
  • Available for domestic and international travel, including overnight stays
  • Valid current passport required
  • Ability to drive and have a valid driver's license
  • Fluent in local office language and in English, both written and verbal
  • Broad knowledge of drug development process and client needs

At Worldwide Clinical Trials, we are committed to fostering an inclusive and equitable workplace by providing transparent compensation.
The salary range for this position is annually (For hourly paid positions, the stated salary range reflects hourly rates):
United States of America - $112,000.00 - $222,000.00
The salary range provided is intended to give candidates an understanding of potential earnings. Compensation will fall within the provided range, and it not a guarantee of exact salary. The final salary will be determined based on relevant experience, performance, education, and internal equity. In addition to base salary, we offer a competitive benefits package depending on location. We ensure pay equity and transparency and comply with all applicable labor laws. Salary information will be discussed during the interview process, and we encourage candidates to inquire about compensation at any stage.
We love knowing that someone is going to have a better life because of the work we do.
To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

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