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Contract Clinical Research Associate Jobs (NOW HIRING)

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

This will be for a 6 month contract. As a Clinical Research Associate at ICON , you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative ...

ClinChoice

ClinChoice is a rapidly growing global contract research organization. We're currently expanding our CRA network in the Netherlands and looking for talented Clinical Research Associates (CRA II and ...

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Contract Clinical Research Associate information

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$12

$41

$69

How much do contract clinical research associate jobs pay per hour?

As of Aug 2, 2026, the average hourly pay for contract clinical research associate in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.

What are some of the unique challenges faced by Contract Clinical Research Associates compared to permanent employees?

Contract Clinical Research Associates often need to quickly adapt to new study protocols, sponsor requirements, and team dynamics since they may work on multiple projects for different organizations. This can mean a faster onboarding process and the need to build rapport with new colleagues and site staff efficiently. Additionally, contract CRAs must be highly organized to manage shifting assignments and maintain compliance across different trial sites, as well as keep up with varying documentation standards. While this variety can be rewarding, it can also present challenges in terms of consistency and long-term project ownership.

What are Contract Clinical Research Associates?

Contract Clinical Research Associates (CRAs) are professionals who monitor clinical trials on behalf of pharmaceutical companies, contract research organizations (CROs), or other sponsors, but work on a contract or freelance basis rather than as permanent employees. Their primary responsibilities include ensuring that trials are conducted according to regulatory guidelines, monitoring data accuracy, and verifying that patient rights and safety are protected. Contract CRAs may work on multiple projects for different clients and often enjoy more flexibility in their schedules and work locations. This role requires strong organizational skills, knowledge of Good Clinical Practice (GCP), and the ability to travel to clinical sites.

What are the key skills and qualifications needed to thrive as a Contract Clinical Research Associate, and why are they important?

To thrive as a Contract Clinical Research Associate, you need a solid understanding of clinical trial protocols, regulatory guidelines (such as GCP and ICH), and typically a degree in life sciences or related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are highly valued. Strong attention to detail, organizational skills, and effective communication help build productive site relationships and ensure compliance. These skills are crucial for maintaining data integrity, ensuring regulatory adherence, and supporting successful clinical trial outcomes.

What is the difference between Contract Clinical Research Associate vs Clinical Research Associate?

AspectContract Clinical Research AssociateClinical Research Associate
CredentialsTypically requires a degree in life sciences and relevant certificationsSame as Contract CRA, often with additional experience
Work EnvironmentTemporary, project-based assignments often with multiple sponsorsFull-time employment with a single organization or sponsor
Employer & Industry UsageUsed by CROs and pharma companies for short-term projectsCommonly employed directly by pharmaceutical companies or CROs
Search & Comparison IntentOften compared for flexibility and contract work benefitsViewed as a permanent role with career growth

In summary, Contract Clinical Research Associates work on temporary, project-specific basis, often with multiple sponsors, offering flexibility. Clinical Research Associates typically hold full-time roles within a single organization, providing stability and career development opportunities.

More about Contract Clinical Research Associate jobs
What cities are hiring for Contract Clinical Research Associate jobs? Cities with the most Contract Clinical Research Associate job openings:
What states have the most Contract Clinical Research Associate jobs? States with the most job openings for Contract Clinical Research Associate jobs include:
What job categories do people searching Contract Clinical Research Associate jobs look for? The top searched job categories for Contract Clinical Research Associate jobs are:
Contract Clinical Research Associate jobs near you
Infographic showing various Contract Clinical Research Associate job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 69% Full Time, 28% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

In-house Sr Clinical Research Associate

Solomon Page

San Diego, CA • On-site

$60 - $75/hr

Contractor

Medical, Dental, Vision, Retirement

Re-posted 25 days ago

Job description

A clinical-stage biopharmaceutical company in San Diego, California is seeking an experienced Contract Clinical Research Associate (CRA) to support ongoing clinical trials. This is an in-house clinical operations role (not a field monitoring position) with minimal travel required.
  • Pay rate: $60-75/hour
  • Location: California or Remote with travel to CA

Responsibilities:
  • Support clinical operations across multiple studies while ensuring subject safety and data integrity
  • Review and maintain the electronic Trial Master File (eTMF) in compliance with SOPs, GCP, and ICH guidelines
  • Support study start-up and ongoing trial activities, including regulatory documentation and site readiness
  • Serve as a liaison between internal teams, CROs, vendors, and investigator sites
  • Review monitoring visit reports (PSV, SIV, IMV, COV)
  • Remotely track enrollment and treatment status using IxRS and EDC systems
  • Maintain study tracking tools, meeting minutes, and action items
  • Participate in investigator meetings, study training, and co-monitoring activities as needed
  • Perform duties in compliance with FDA regulations, ICH-GCP, and company policies

Required Qualifications:
  • Bachelor's degree preferred
  • 4 years of In house CRA experience
  • Sponsor experience required
  • Site management and CRO/vendor oversight
  • Proficiency with Microsoft Office and Veeva eTMF required
  • Smartsheet and SharePoint a plus
  • Phase I-III Experience
    Clinical Resource Network Distinction
    CRN, a division of Solomon Page, offers a comprehensive benefits program for hourly employees. We pride ourselves on offering medical, dental, vision, 401(k), telehealth services, ESOP, and commuter benefits to our employees, including consultants - which sets us apart in the industries we serve.
    About CRN
    Founded in 2002, Clinical Resource Network (CRN), a division of Solomon Page, provides clinical research and talent solutions for pharmaceutical, biotech, and medical device companies. Focused on forming long-term relationships, services encompass contract staffing, project staffing, consultative services, and full-time placements. For more information, visit https://www.solomonpage.com/crn and connect with us on Facebook and LinkedIn .
    Opportunity Awaits.
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