ZipRecruiter

Log In

1

Freelance Clinical Research Associate Jobs (NOW HIRING)

ICON

Clinical Research Associate

Clinical Research Associate - Multi TA/Oncology - US ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients ...

Tigermed America

Be Seen First

Clinical Research Associate

Denver, CO · On-site

Senior Clinical Research Associate As Clinical Research Associate you will be responsible for monitoring clinical trials and ensuring investigators are conducting the research within requirements of ...

ClinChoice

Senior Clinical Research Associate

Key words: Clinical Research Associate, CRA, Freelance, Permanent, CRO, Contract Research Organization, Outsourced, Outsourcing, Oncology, Monitoring, Early Phase Oncology Trials, Senior CRA ...

ClinChoice

Senior Clinical Research Associate

Key words: Clinical Research Associate, CRA, Freelance, Permanent, CRO, Contract Research Organization, Outsourced, Outsourcing, Oncology, Monitoring, Early Phase Oncology Trials, Senior CRA ...

RevBio, Inc.

Clinical Research Associate

Lowell, MA · On-site

The Clinical Research Associate will support the execution and oversight of clinical studies across multiple indications and geographic regions, including the United States, Europe, and the United ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings Available* Position Location: 541 Church at North Hills St., Suite 1000, Raleigh, NC 27609 *100% Remote ...

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP ...

WEP Clinical

Senior Clinical Research Associate

The WEP Clinical Senior Clinical Research Associate (Senior CRA) oversees all aspects of clinical monitoring and site management in compliance with GCP, global regulatory requirements, and WEP ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site

Parexel International LLC Position Title: Sr. Clinical Research Associate *Multiple Openings Available* Position Location: 541 Church at North Hills St., Suite 1000, Raleigh, NC 27609 *100% Remote ...

RevBio, Inc.

Clinical Research Associate

Lowell, MA · On-site

The Clinical Research Associate will support the execution and oversight of clinical studies across multiple indications and geographic regions, including the United States, Europe, and the United ...

RevBio, Inc.

Clinical Research Associate

Lowell, MA · On-site

The Clinical Research Associate will support the execution and oversight of clinical studies across multiple indications and geographic regions, including the United States, Europe, and the United ...

RevBio, Inc.

Clinical Research Associate

Lowell, MA · On-site

The Clinical Research Associate will support the execution and oversight of clinical studies across multiple indications and geographic regions, including the United States, Europe, and the United ...

previous page

Showing results 41-60

All Jobsfreelance JobsFreelance Clinical Research Associate Jobs

Freelance Clinical Research Associate information

See salary details

$36K

$94.3K

$143.5K

How much do freelance clinical research associate jobs pay per year?

As of Aug 23, 2026, the average yearly pay for freelance clinical research associate in the United States is $94,314.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,500.00 and $128,000.00 per year, depending on experience, location, and employer.

What is a freelance clinical research associate?

A Freelance Clinical Research Associate (CRA) is an independent professional who monitors clinical trials to ensure compliance with regulatory guidelines, protocols, and Good Clinical Practice (GCP). Unlike full-time CRAs, freelancers work on a contract basis for multiple sponsors, contract research organizations (CROs), or clinical sites. Their responsibilities include site visits, data verification, risk assessment, and communication with investigators. This role offers flexibility, diverse project opportunities, and control over workload but requires strong self-management and networking skills.

What are the key skills and qualifications needed to thrive as a freelance clinical research associate?

To thrive as a Freelance Clinical Research Associate, you need a strong background in clinical research, understanding of ICH-GCP guidelines, and typically a relevant life sciences degree. Familiarity with electronic data capture (EDC) systems, trial management software, and certifications such as GCP training are commonly expected. Excellent organizational skills, self-motivation, and clear communication are essential soft skills for managing independent workloads and liaising with multiple stakeholders. These abilities ensure regulatory compliance, accurate data collection, and successful coordination of clinical trials across diverse settings.

What are the typical challenges faced by freelance clinical research associates, and how can they be managed?

As a freelance Clinical Research Associate, you'll often manage multiple studies or sites at once, requiring strong time management and organizational skills. Challenges can include juggling different sponsor requirements, keeping up with regulatory changes, and maintaining clear communication across virtual teams. Effective use of project management tools, regular updates with stakeholders, and continuous professional development help address these challenges. Freelancers often enjoy greater flexibility but must proactively seek new contracts and networking opportunities to maintain steady work. Being adaptable and detail-oriented are key traits to thrive in this dynamic environment.

More about Freelance Clinical Research Associate jobs

What cities are hiring for Freelance Clinical Research Associate jobs?

Cities with the most Freelance Clinical Research Associate job openings:

What are the most commonly searched types of Freelance Clinical Research jobs?

The most popular types of Freelance Clinical Research jobs are:

What states have the most Freelance Clinical Research Associate jobs?

States with the most job openings for Freelance Clinical Research Associate jobs include:

What job categories do people searching Freelance Clinical Research Associate jobs look for?

The top searched job categories for Freelance Clinical Research Associate jobs are:

Freelance Clinical Research Associate jobs near you
Infographic showing various Freelance Clinical Research Associate job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $94,314 per year, or $45.3 per hour.

Clinical Research Associate

Medasource

North Chicago, IL • On-site

Other

Posted 11 days ago

Job description

Title: Clinical Research Associate

Duration: 1 year contract (potential of extension)

Location: Remote with up to 75% travel


Job Description:

Abbott's Core Diagnostics team is seeking a Clinical Research Associate to support a Traumatic Brain Injury (TBI) clinical research initiative. This individual will support multi-site clinical trial operations while ensuring strict compliance with protocol in a highly regulated environment. The ideal candidate brings strong monitoring fundamentals, exceptional attention to detail, and the ability to operate independently across multiple sites and stakeholders.


Responsibilities:

  • Perform site qualification, initiation, interim monitoring, and close-out visits across assigned clinical sites
  • Support oversight of approximately 4-5 clinical research sites, including primary and secondary site responsibilities
  • Ensure protocol compliance, GCP adherence, and accurate study documentation
  • Conduct source data verification/review and investigational product accountability activities
  • Identify, document, and escalate site issues, deviations, and risks appropriately
  • Complete detailed trip reports, monitoring documentation, and required reporting within established timelines
  • Collaborate cross-functionally with clinical operations, investigators, and study coordinators
  • Support multiple studies simultaneously as needed
  • Maintain compliance with time tracking, reporting, and data handling procedures

Qualifications:

  • 3-5+ years of clinical research experience preferred
  • Open to candidates with:
  • CRA experience within sponsor environments
  • Strong clinical research coordinator experience from hospital or academic settings
  • Strong understanding of:
  • Site monitoring activities
  • Source data verification/review
  • Investigational product accountability
  • GCP and clinical trial documentation requirements
  • Excellent written and verbal communication skills
  • Strong critical thinking and situational problem-solving abilities
  • Ability to work independently and manage competing priorities across multiple sites
  • Highly organized with strong time management skills
  • Ability to travel nationally up to 75% as required
  • Comfortable operating within a 40-hour work week structure


Apply