Job Description

Clinical Research Associate (CRA)
Remote | 5-Month Assignment (potential to extend / convert)
Target Start: January 5
Rate: $35-$45/hr

Travel: Up to 15% (WA, CA, MN, MD, KY)
A leading global provider of life science research and clinical diagnostic solutions is seeking a Clinical Research Associate (CRA) to support an upcoming QC-focused clinical study.
As a CRA, you will play a key role in ensuring the successful execution of clinical trials from initiation through closeout. You will work closely with investigators, study coordinators, and internal partners across R&D, Finance, Marketing, and other core functional teams. Your day-to-day activities will center on data entry, data organization, routine site monitoring, and maintaining essential study documentation.
How You'll Make an Impact

• Conduct Site Initiation Visits (SIVs), Routine Monitoring Visits (RMs), and Closeout Visits to ensure adherence to protocols, GCP, and regulatory standards
• Perform source data verification, data collection, and manage query resolution
• Maintain and manage study documentation, including regulatory files and the Trial Master File (TMF)
• Collaborate with cross-functional teams to support timely study execution
• Prepare and submit monitoring visit reports, follow-up letters, and related study documentation

What You Bring

• Bachelor's degree required
• 1-2 years of experience as a CRA or in a similar clinical research role
• Strong understanding of clinical trial processes, regulations, and ICH-GCP guidelines
• Excellent organizational, communication, and time-management skills
• CRA certification is a plus

Please submit your resume in Word or PDF format to be considered.

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