In-house Sr Clinical Research Associate
Clinical Resource Network (CRN)
Behavioral Health Market Context
Apply Nowvia LinkedIn
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.
• 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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