California Licensed Clinical Research Associate

A company is looking for a Clinical Research Associate (Contractor).

Key Responsibilities

Ensure compliance with clinical trial protocols and regulatory obligations during site monitoring

Conduct on-site and remote monitoring activities, including source document verification

Write and submit reports on investigational site findings and update tracking systems

Required Qualifications

Minimum Bachelor's degree in a life science-related field, RN certification, or equivalent

3+ years of experience in a clinical trials research environment, with in vitro diagnostics study experience

General knowledge of regulatory requirements and Good Clinical Practice (GCP)

High proficiency in Veeva Vault and Medrio

CRA certification by a recognized professional organization is a plus