CRA 1, IQVIA Biotech

Lifelancer
San Francisco, CA
Category Research
Job Description
The Clinical Research Associate I (CRA I) plays a key role in supporting the successful conduct of clinical research studies by performing site monitoring and site management activities. In this position, you will ensure that assigned study sites conduct trials in compliance with the protocol, applicable regulations, Good Clinical Practice (GCP), and ICH guidelines. This role is essential in protecting patient safety, ensuring high-quality clinical data, and maintaining study integrity.

Requirements

  • Conduct various types of monitoring visits including site selection, initiation, routine monitoring, and close-out visits to evaluate the quality and integrity of site practices
  • Verify that study activities are performed according to regulatory requirements and sponsor expectations, escalating quality concerns as necessary
  • Build and maintain strong communication with investigative sites, providing protocol training, setting expectations, addressing site-level challenges, and supporting recruitment planning
  • Collaborate closely with internal project teams to ensure cohesive study execution and contribute to site-level financial processes or start-up activities as needed

Benefits

  • Generous Paid Time Off
  • 401k Matching
  • Health and welfare benefits
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