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Freelance Clinical Project Manager Jobs (NOW HIRING)

Laborie

Clinical Project Manager

Minnetonka, MN · On-site

$130K - $135K/yr

As a key member of the Clinical team, theClinical Project Manager (CPM)is responsible for the management of all aspects of Clinical Trial Team activities for assigned project(s). The CPM , in concert ...

Emerus

... project manager in healthcare, strongly preferred * Bachelor's Degree or higher required * PMP required * Clinical licensure or relevant clinical credential required (e.g. RN, LVN, ARRT, RRT/CRT ...

Emerus

Clinical Project Manager

... project manager in healthcare, strongly preferred * Bachelor's Degree or higher required * PMP required * Clinical licensure or relevant clinical credential required (e.g. RN, LVN, ARRT, RRT/CRT ...

Collabera

Clinical Project Manager

North Chicago, IL · On-site

... Clinical Teams, and Public Affairs). Applies knowledge across multiple therapeutic areas to support ... Appropriately advises management of project risks and presents recommendations for resolution.

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

As of Aug 13, 2026, the average hourly pay for freelance clinical 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 is a freelance clinical project manager?

A Freelance Clinical Project Manager oversees clinical trials and research projects on a contractual basis. They ensure studies comply with regulations, manage timelines and budgets, coordinate teams, and communicate with stakeholders. Unlike full-time employees, they work independently and may juggle multiple projects from different sponsors or CROs. Their expertise helps companies efficiently execute clinical trials while maintaining flexibility in staffing.

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

A Freelance Clinical Project Manager requires expertise in clinical trial management, regulatory compliance, protocol development, and budgeting, often supported by a science degree and several years of experience in clinical research. Familiarity with tools like clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as PMP or GCP are highly valued. Outstanding organization, problem-solving, and interpersonal skills help them coordinate diverse teams and manage multiple projects simultaneously. These skills are crucial for ensuring trials are completed on time, within budget, and in accordance with industry regulations.

What are the common challenges faced by freelance clinical project managers, and how can I prepare for them?

Freelance clinical project managers often encounter challenges such as coordinating across geographically dispersed teams, adapting to varying sponsor requirements, and ensuring timely regulatory submissions. You can prepare by staying updated on industry best practices, strengthening your project management and communication skills, and building familiarity with multiple clinical trial management platforms. Successfully navigating these challenges relies on proactive planning, flexibility, and establishing clear communication channels with all stakeholders. Many freelancers also build strong professional networks to access additional support and resources when needed.

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Freelance Clinical Project Manager jobs near you
Infographic showing various Freelance Clinical Project Manager job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 86% Full Time, 12% Part Time, and 1% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $126,262 per year, or $60.7 per hour.

Senior Clinical Project Manager

Icon plc

Blue Bell, PA • Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 13 days ago

Job description

Senior Clinical Project Manager (Oncology) - Remote, US

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Senior Clinical Project Manager at ICON, you will be responsible for leading and manage projects, ensuring successful execution and delivery of project objectives, including those supporting radiopharmaceutical and radioligand-based clinical programs.

What You Will Do:

You will manage day-to-day project and program management activities, supporting your team to deliver quality outcomes.
Key responsibilities include:

  • Developing and executing clinical project plans, focusing on achieving project goals and objectives, including those for radiopharmaceutical and radioligand studies with specialized operational requirements.

  • Leading cross-functional teams to ensure the successful implementation of project activities.

  • Collaborating with stakeholders to identify project requirements and define project scope.

  • Mentoring and guiding team members, fostering a culture of excellence and continuous improvement.

  • Driving the development of project documentation and reports to present findings to stakeholders in a clear and actionable manner.

  • Staying abreast of industry trends and emerging technologies, including advancements in precision medicine, radiopharmaceuticals, and targeted oncology therapies, to integrate best practices into project management strategies.

  • Contributing to organizational growth through effective project leadership and strategic planning.

Your Profile:

You will have solid clinical project and program management experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field

  • Extensive experience in project management, with a proven track record of leading successful projects in the pharmaceutical or biotech industry;

    experience in oncology, nuclear medicine, radiopharmaceuticals, or radioligand therapies is strongly preferred

  • Strong proficiency in project management tools and methodologies, with excellent attention to detail.

  • Excellent analytical and problem-solving skills, with the ability to develop effective project strategies.

  • Demonstrated leadership skills, with experience in managing and mentoring teams effectively.

  • Exceptional communication skills, with the ability to convey technical concepts to diverse audiences.

  • Detail-oriented, with strong organizational skills to manage multiple projects and deadlines in a dynamic environment.

  • Willingness to travel as required (approximately 25%)

#LI-MH1

#LI-REMOTE


Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.


If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.

Are you a current ICON Employee? Please click here to apply

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