In-house Sr Clinical Research Associate

Clinical Resource Network (CRN)

San Diego, CAContractorPosted Jun 5, 2026

Behavioral Health Market Context

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Benefits

Pay rate: $60-75/hourWe 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

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: San Diego, 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
• 3 years of CRA experience
• 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.

Qualifications

  • 3 years of CRA experience
  • Site management and CRO/vendor oversight
  • Proficiency with Microsoft Office and Veeva eTMF required
  • Phase I–III Experience

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


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