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Procter & Gamble

Clinical Trial Manager

Mason, OH · On-site

A P&G Clinical Trial Manager will be responsible for: * Design, implementation, and management of ... P&G's freelancer opportunities are for project-based or other short-term engagements that require ...

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How much do freelance clinical jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for freelance clinical in the United States is $47.71, according to ZipRecruiter salary data. Most workers in this role earn between $24.28 and $61.78 per hour, depending on experience, location, and employer.

What is a Freelance Clinical job?

A Freelance Clinical job typically involves providing clinical or healthcare-related services on a contract or per-project basis rather than as a full-time employee. Freelance clinical professionals may include nurses, medical writers, clinical research associates, or healthcare consultants. They often work with hospitals, research organizations, or pharmaceutical companies, offering expertise in areas like patient care, clinical trials, or medical documentation. This role provides flexibility and independence but may require managing multiple clients and maintaining necessary certifications.

What are the key skills and qualifications needed to thrive in the Freelance Clinical position, and why are they important?

To excel as a Freelance Clinical professional, you typically need a background in a relevant healthcare field such as nursing, clinical research, or therapy, along with applicable licenses or certifications. Familiarity with electronic health record systems, clinical trial management software, and regulatory compliance tools is often necessary. Strong organizational skills, proactive communication, and the ability to work independently are crucial soft skills for managing multiple clients and projects. These competencies enable reliable, high-quality clinical service delivery and foster client trust in a flexible, self-directed work environment.

What are the unique challenges of working as a Freelance Clinical professional compared to traditional clinical roles?

As a Freelance Clinical professional, you may encounter challenges such as managing fluctuating workloads, handling multiple clients simultaneously, and ensuring consistent access to up-to-date resources and professional development. Unlike traditional clinical roles that offer established support systems, freelancers are responsible for their own scheduling, billing, and compliance with changing regulations. However, this independence also offers flexibility and the opportunity to diversify your experience across different settings. Success often relies on strong self-motivation, organization, and effective client communication.

More about Freelance Clinical jobs
What cities are hiring for Freelance Clinical jobs? Cities with the most Freelance Clinical job openings:
What are the most commonly searched types of Clinical jobs? The most popular types of Clinical jobs are:
What states have the most Freelance Clinical jobs? States with the most job openings for Freelance Clinical jobs include:
What job categories do people searching Freelance Clinical jobs look for? The top searched job categories for Freelance Clinical jobs are:
Freelance Clinical jobs near you
Infographic showing various Freelance Clinical job openings in the United States as of June 2026, with employment types broken down into 5% Locum Tenens, 2% Full Time, 4% Part Time, 2% Temporary, 85% Contract, and 2% Nights. Highlights an 86% Physical, 1% Hybrid, and 13% Remote job distribution, with an average salary of $99,230 per year, or $47.7 per hour.

FREELANCE Clinical Research Associate

SanaClis

Philadelphia, PA • On-site

Other

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

We are looking for a Freelance, Part-Time CRA located on the U.S. East Coast to support and strengthen our Clinical Operations team.


Job Requirements:


  • Bachelor’s degree required – preferred qualification in life sciences or medical sciences
  • Minimum 3 years of experience of onsite monitoring activities
  • Profound knowledge of clinical research processes and medical terminology
  • Expert knowledge of ICH GCP, and international and local regulatory requirements
  • Passion for clinical research
  • English language proficiency of minimum level C1 (ref. CEFR) – fluent in written and spoken English
  • Driving license B and ability to travel

Job Responsibilities:


  • You would be primarily responsible for monitoring clinical trials and
  • Ensuring that clinical trial is conducted, recorded, and reported in accordance with all applicable international and local regulations and guidelines, good practices, SOPs and Clinical Trial Protocol
  • Ensuring data quality and integrity meet acceptable clinical standards
  • Guaranteeing the rights and safety of patients involved in a study are protected
  • Performing and coordinating all aspects of the clinical monitoring and site management process
  • Conducting remote and on-site visits to assess protocol and regulatory compliance and managing required documentation
  • Developing collaborative relationships with investigational sites, act as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects rights, well-being, and data reliability; and you would ensure audit readiness.
  • Serving as facilitator of Clinical Trial conduct in respective area in terms of identifying qualified sites and investigators, facilitating communication between sponsor and regulatory authorities and trial sites.


What We Offer:


  • Competitive salary
  • Friendly environment in a privately owned international company
  • Additional benefits will be discussed during the interview


You can apply via the link or send a CV directly to: careers@sanaclis.com


* SanaClis is an equal employment opportunity employer. We value diversity and are committed to creating an inclusive environment for all employees. All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity or expression, religion, national origin, ancestry, age, disability, marital status, pregnancy, protected veteran status, order of protection status, protected genetic information, or any other characteristic protected by law.

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