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Clinical Trial Project Manager Jobs (NOW HIRING)

Kardigan

Clinical Trial Manager

Princeton, NJ · Remote

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... This role is pivotal in ensuring key project deliverables, primarily from CROs and vendors, are met ...

Hirebridge

$125 - $150/hr

This role is suited to someone who is passionate about clinical trial project management, eager to keep learning, and ready to take ownership in a supportive environment. You will have access to ...

Kardigan

Clinical Trial Manager

Princeton, NJ · On-site

As a Clinical Trial Manager (CTM), you will be part of the Clinical Operations team reporting to ... This role is pivotal in ensuring key project deliverables, primarily from CROs and vendors, are met ...

Aerogen Pharma Limited

$125 - $150/hr

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials ... project management skills, as well as a deep understanding of the regulations and ethical ...

Verastem

Clinical Trial Manager

Boston, MA · On-site

$100K - $125K/yr

Works with senior Clinical Operations members to lead the clinical project team members in the ... Global Phase 3 clinical trial management experience * Minimum of 3 years of clinical trial ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead ... Strong project management skills with the ability to manage multiple trials simultaneously.

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead ... Strong project management skills with the ability to manage multiple trials simultaneously.

Clinovo

Clinical Trial Manager

Waltham, MA · On-site

Leveraging a strong understanding of clinical trial execution, the CTM will oversee day-to-day clinical trial operations, including clinical project management, study site activities, CRA monitoring ...

C4 Therapeutics Inc

Clinical Trial Manager

Watertown, MA · On-site

$138K - $153K/yr

... project management, and leadership capabilities. * Demonstrated experience with contributing to ... Preferred: * Experience with oncology clinical trial management and/or global clinical trials.

Scorpion Therapeutics

Global Study Leader

California, MD · On-site

$150 - $200/hr

Strong knowledge of clinical trial processes, ICH-GCP, regulatory requirements, and regulatory start-up planning (SSU). * Proven cross-functional and global, multi-center trial project management.

C4-Therapeutics-Inc

Clinical Trial Manager

Watertown, MA · On-site

$125 - $150/hr

Clinical Trial Manager Full Time Management Watertown, MA, US 23 days ago Requisition ID: 1144 ... project management, and leadership capabilities. * Demonstrated experience with contributing to ...

Aerogen

Clinical Trial Manager

Morrisville, NC · On-site

$100 - $125/hr

The Clinical Trial Manager (CTM) is responsible for managing various aspects of clinical trials ... The role requires leadership, effective communication, project management skills, and a deep ...

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

As of Sep 9, 2026, the average hourly pay for clinical trial project manager in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What does a clinical trial project manager do?

A Clinical Trial Project Manager oversees the planning, implementation, and management of clinical trials to ensure they are conducted efficiently, on time, and in compliance with regulatory standards. They coordinate between various teams, manage budgets and timelines, and ensure that study protocols are followed. Their role is crucial to the successful completion of clinical research, which ultimately supports the development of new medical treatments and drugs.

What are the key skills and qualifications needed to thrive as a clinical trial project manager?

To thrive as a Clinical Trial Project Manager, you need strong project management skills, a solid understanding of clinical research protocols, and often a background in life sciences or a related field. Familiarity with tools like CTMS (Clinical Trial Management Systems), EDC (Electronic Data Capture), and certifications such as PMP or ACRP are highly valued. Exceptional communication, leadership, and problem-solving abilities help you coordinate cross-functional teams and address challenges efficiently. These competencies are crucial to ensure trials are conducted on time, within budget, and in compliance with regulatory standards.

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

Clinical Trial Project Managers often encounter challenges such as maintaining consistent communication across all sites, ensuring regulatory compliance in different regions, and managing timelines while balancing site-specific issues. Coordinating multiple teams and vendors can be complex, requiring strong organizational skills and proactive problem-solving. Despite these challenges, the role provides valuable opportunities to develop leadership skills and gain exposure to a wide range of clinical research operations.

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

AspectClinical Trial Project ManagerClinical Research Coordinator
CredentialsBachelor's degree; often PMP or related certificationsBachelor's degree in health or related field; often certifications like CCRP
Work EnvironmentOversees multiple trials, manages teams, coordinates with sponsorsWorks directly with participants, manages daily trial activities at sites
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch hospitals, academic institutions, clinical sites
Search & Comparison IntentUnderstanding managerial roles in clinical trialsDetails on site-level trial coordination

The Clinical Trial Project Manager focuses on overseeing entire clinical trials, managing teams, and coordinating with sponsors. In contrast, the Clinical Research Coordinator handles day-to-day trial activities at the site level, working directly with participants. Both roles require relevant certifications and are essential in the clinical research process, but they differ in scope and responsibilities.

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Clinical Trial Project Manager jobs near you
Infographic showing various Clinical Trial Project Manager job openings in the United States as of September 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Trial Project Manager - Cardiovascular, Renal, Gastrointestinal - Cincinnati

Cincinnati, OH • On-site

Medpace, Inc.
Medical Equipment and Supplies Manufacturing • 1 - 5K employees
Learn more about Medpace, Inc.external

Other

Medical, Retirement, PTO

Re-posted 11 days ago

Medpace rating

8.6

Company rating: 8.6 out of 10

Based on 12 frontline employees who took The Breakroom Quiz

16th of 75 rated research

Job description

Job Summary
Medpace is the leading CRO for Biotech companies and is continuing to add established Clinical Trial Managers and Project Managers with a focus on Cardiovascular, Renal, and Gastrointestinal therapeutic areas to join our Clinical Trial Management Group. We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.
Responsibilities
  • Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
  • Serve as primary Sponsor contact for operational project-specific issues and study deliverables
  • Maintain in depth knowledge of protocol, therapeutic area, and indication
  • Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
  • Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
  • Develop operational project plans
  • Manage risk assessment and execution
  • Responsible for management of study vendor
  • Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables

Qualifications
  • Bachelor's degree in a health-related field; Advanced degree in a health-related field preferred
  • Experience in Phases 1-4; Phases 2-3 preferred
  • 3-5 years as a project/clinical trial manager within a CRO;
  • Management of overall project timeline
  • Strong leadership skills

Medpace Overview
Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries.
Why Medpace?
When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Purpose-Driven Work
    • Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence

Collaborative Culture
    • Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
    • Leadership throughout Medpace is both accessible and approachable

Continuous Growth & Development
    • Office based environment with on-site mentors
    • Defined career paths with clear advancement opportunities
    • Industry renowned onboarding and training programs designed to accelerate professional development
    • Ongoing training and continuous learning opportunities throughout your career
    • An environment that encourages employees to influence change, contribute ideas, and grow quickly

Other Employee Benefits
    • Competitive compensation programs that recognize and reward performance
    • Comprehensive health, wellness, retirement, and PTO benefits
    • Office based culture with occasional WFH that provides flexibility for eligible positions after training
    • Company-sponsored social events and intramural sports

Cincinnati Headquarters Experience
    • A modern corporate campus designed to support collaboration and productivity
    • Multiple on-site dining options in the heart of Madison Square
    • Free on-site parking
    • Convenient access to on-site 24-7 fitness and wellness facilities

What to Expect Next
A Medpace team member will review your application and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.

What Medpace employees say

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About Medpace

Sourced by ZipRecruiter

Medpace is a globally recognized clinicial contract research organization (CRO) based in Cincinnati, OH, in the United States. Established in 1992, it operates in the healthcare sector, providing scientifically-driven outsourcing solutions for the development of drugs and medical devices. It offers comprehensive services like full-service clinical development services, regulatory affairs management, clinical pharmacology, data management, statistical analysis, and medical writing. By applying a scientifically-driven, therapeutically-focused, and patient-centric approach, Medpace's mission is to accelerate the global development of safe and effective medical therapies.

Industry

Medical equipment and supplies manufacturing

Company size

1,001 - 5,000 Employees

Headquarters location

Cincinnati, OH, US

Year founded

1992

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