Clinical Research Associate II, Phase I - California Job at Fortrea, San Diego, CA

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  • Fortrea
  • San Diego, CA

Job Description

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.

Responsibilities

  • 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

Requirements

  • 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

Compensation: $100,000-$120,000

Job Tags

Local area, Night shift

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