Clinical Research Associate II, Phase I - California
Fortrea · San Diego, CA
Clinical OperationsFull timeCompany career page
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Role summary
Fortrea seeks a Clinical Research Associate II with Phase I experience to manage study site monitoring, regulatory compliance, and data integrity for clinical trials. The role is based in California and requires 1+ years of clinical monitoring experience with significant travel.
What they're looking for
- University or college degree or allied health certification from accredited institution
- 1+ years of clinical monitoring experience
- Phase I trial experience
- 40-50% overnight travel capability
- Proficiency with electronic data management systems
- Valid driver's license and ability to operate vehicle safely
What you'll be doing
- Conduct routine monitoring and close-out of clinical study sites, including pre-study and initiation visits
- Verify informed consent procedures and protocol adherence per regulatory requirements
- Review Case Report Forms and source documents for data integrity, query generation, and resolution
- Complete Serious Adverse Event reporting and follow-up documentation
- Coordinate clinical projects as Local Project Coordinator with site liaison responsibilities
Compensation$100,000-$120,000
Privacy & handoff
This role links to Fortrea's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.