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Freelance Remote Clinical Trials Jobs (NOW HIRING)

Adecco

Clinical Trials Manager- Remote

Chapel Hill, NC · Remote

$62 - $64.73/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Clinical Trials Manager (CTM) Location: Remote Schedule: Full-Time | Eastern Time Zone Hours Pay: $62.00-$64.73 per hour Position Overview We are seeking an experienced Clinical Trials Manager (CTM ...

IQVIA

Freelance Independent Rater

Los Angeles, CA · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Boston, MA · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

London, OH · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Houston, TX · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

New York, NY · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Washington, DC · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

San Francisco, CA · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

New York, NY · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Houston, TX · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Vancouver, WA · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Washington, DC · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Boston, MA · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

London, OH · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Los Angeles, CA · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Chicago, IL · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

Chicago, IL · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

IQVIA

Freelance Independent Rater

New Providence, NJ · Remote

$62K - $156K/yr

... Remote Flexible Working Hours Freelance Contract What We're Looking For Professionals with ... clinical trials * Strong interviewing and assessment skills * Fluent English, any additional ...

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Freelance Remote Clinical Trials information

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$14

$47

$132

How much do freelance remote clinical trials jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for freelance remote clinical trials 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 remote clinical trials specialist?

Freelance remote clinical trials involve independent professionals who work remotely to support or manage various aspects of clinical research studies. These roles can include data management, regulatory documentation, patient recruitment, monitoring, and more, all performed outside of a traditional office or onsite setting. Freelancers in this field often collaborate with pharmaceutical companies, contract research organizations (CROs), and academic institutions, using digital tools to conduct and oversee trial activities from any location. This flexible arrangement allows for a wider range of expertise and can help speed up the clinical trial process. Remote clinical trials are increasingly popular due to advances in technology and the need for decentralized research.

What are the key skills and qualifications needed to thrive as a freelance remote clinical trials specialist?

To thrive as a Freelance Remote Clinical Trials Specialist, you need a background in medical research, clinical trial protocols, and regulatory compliance, often supported by a degree in life sciences or related certification such as GCP (Good Clinical Practice). Familiarity with electronic data capture (EDC) systems, remote monitoring tools, and trial management software is essential. Strong organizational skills, self-motivation, and effective communication set top performers apart, especially when collaborating remotely across teams. These competencies ensure accurate data collection, regulatory adherence, and successful trial outcomes in a flexible, virtual environment.

What are some common challenges faced by freelance remote clinical trials specialists, and how can they be addressed?

Freelance remote professionals in clinical trials often encounter challenges such as coordinating across multiple time zones, maintaining clear communication with dispersed teams, and ensuring compliance with regulatory standards without in-person supervision. To address these issues, it's important to set up reliable digital communication channels, proactively schedule regular check-ins, and stay updated on industry regulations. Utilizing project management and collaboration tools can also streamline workflows and help maintain data integrity throughout the trial process.

What is the difference between Freelance Remote Clinical Trials vs Clinical Research Coordinator?

AspectFreelance Remote Clinical TrialsClinical Research Coordinator
CredentialsVaries; often requires knowledge of clinical trials, certifications optionalTypically requires a bachelor's degree in health or related field, and certification
Work EnvironmentRemote, flexible, project-basedOn-site or hybrid at research sites or hospitals
Employer & Industry UsageFreelance platforms, biotech, pharma companiesHospitals, research institutions, pharmaceutical companies
Search & Comparison IntentHigh overlap in trial management, patient coordination, data collectionFocus on site management, patient interaction, regulatory compliance

Freelance Remote Clinical Trials professionals typically work independently on trial projects, often remotely, with flexible hours. Clinical Research Coordinators usually work on-site at research facilities, managing daily trial activities. Both roles involve clinical trial processes but differ mainly in work setting and employment structure.

More about Freelance Remote Clinical Trials jobs

What cities are hiring for Freelance Remote Clinical Trials jobs?

Cities with the most Freelance Remote Clinical Trials job openings:

What are the most commonly searched types of Remote Clinical Trials jobs?

The most popular types of Remote Clinical Trials jobs are:

What states have the most Freelance Remote Clinical Trials jobs?

States with the most job openings for Freelance Remote Clinical Trials jobs include:

What job categories do people searching Freelance Remote Clinical Trials jobs look for?

The top searched job categories for Freelance Remote Clinical Trials jobs are:

Freelance Remote Clinical Trials jobs near you
Infographic showing various Freelance Remote Clinical Trials job openings in the United States as of August 2026, with employment types broken down into 4% As Needed, 70% Full Time, 17% Part Time, and 9% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $99,230 per year, or $47.7 per hour.

Clinical Lead / Clinical Trial Manager - Talent Pipeline Opportunity

Emerald Clinical Trials

Remote

$130K - $160K/yr

Full-time

Posted 9 days ago

Job description

Who We Are
Emerald Clinical Trials is a global leader in clinical research, partnering with over 160 biotech companies and 15 of the world's top 20 pharmaceutical firms. Headquartered in Singapore, we combine scientific excellence with operational expertise to deliver end-to-end clinical trial solutions across all phases, offering Phase I-IV and real-world studies.
With over 25 years of experience and a world-renowned focus in renal research, Emerald Clinical has helped drive medical breakthroughs through deep scientific insight, flawless execution, and an unwavering commitment to quality.
Global Expertise. Local Insight. Real Impact.
Emerald Clinical is where science, speed, and strategy come together to transform healthcare. For over 25 years, we have led the way in clinical research, combining global reach with deep Asia-Pacific expertise and unparalleled local insight to deliver smarter trials and stronger outcomes.
Our 800+ employees that span across Asia-Pacific, Europe, and the Americas are embedded in communities worldwide. We drive faster recruitment, deeper patient engagement, and meaningful results that move medicine forward.
About the Role
As part of our strategic growth plans in the United States, Emerald Clinical Trials is building a network of experienced Clinical Leads / Clinical Trial Managers for upcoming opportunities.
Please note: This is a pipelining advertisement. While active hiring needs may vary, we are eager to connect with talented professionals interested in future opportunities as new studies are awarded.
This home-based position offers the opportunity to oversee global and regional clinical studies, with a strong preference for candidates who bring experience within renal, oncology, cardiometabolic & autoimmune diseases.
Your Responsibilities
  • Manage operational aspects of clinical trials from initiation through completion.
  • Oversee sites and CRA performance.
  • Monitor timelines, study metrics, and recruitment performance.
  • Lead investigator and sponsor interactions.
  • Coordinate study teams and cross-functional activities.
  • Support vendor oversight and issue resolution.
  • Ensure compliance with FDA requirements, GCP, and company SOPs.
  • Contribute to project planning and study execution strategies.

About You
  • Bachelor's degree in a scientific or healthcare discipline.
  • Prior experience as a Clinical Trial Manager, Clinical Lead or equivalent.
  • Strong operational knowledge of site management and monitoring.
  • Excellent understanding of FDA regulations and GCP guidelines.
  • Ability to manage multiple studies and competing priorities.
  • Strong interpersonal and stakeholder-management skills.
  • Experience in renal/nephrology clinical trials is highly preferred.
  • Willingness to travel when required.

Why Join Us?
At our core, Emerald Clinical Trials is committed to transforming clinical research by putting people first - both patients and our employees. By joining our team, you'll be part of a global network of passionate professionals working together to deliver better research and outcomes for millions worldwide.
Here's what makes us stand out:
• Purpose-Driven Work: You'll contribute to clinical trials that genuinely improve lives, with a focus on therapies in renal, cardiometabolic, and oncology.
• Global Reach, Local Expertise: Our teams connect with local communities, building trust and meaningful engagement for every trial.
• Collaboration and Innovation: Work in a culture that values diverse perspectives and creative solutions to solve global health challenges.
What We Offer
We understand that great work happens when people feel valued and supported. That's why we provide:
• Competitive Compensation: A tailored salary and benefits package to reflect your skills and experience.
• Flexibility: Enjoy hybrid or remote working arrangements, depending on your location and role.
• Career Growth: Access to a wealth of learning opportunities and a global network of scientific leaders to help you grow and develop in your role.
• Employee Wellbeing: Participate in programs and initiatives designed to promote work-life balance, health, and team connection, including global engagement surveys, recognition programs, and team-building events.
• Global Opportunities: Be part of a company with international reach, offering you exposure to diverse projects and clients.
Interested? Apply now and help us achieve our mission to improve the health of millions worldwide.
We are an equal-opportunity employer and encourage applications from all qualified candidates.
The expected salary range for this position is $130,000 - $160,000 per year, depending on experience and qualifications.
Department Clinical Operations Role Clinical Lead Locations United States Remote status Fully Remote

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