Clinical Research Associate II, Phase I - California

$100k - $120k

Fortrea

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

Apply

Vacancy posted 14 days ago

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