Sr. Clinical Research Associate, IQVIA

Lifelancer
Lexington, KY
Job Description
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Key responsibilities include site monitoring visits, adapting and tracking subject recruitment plans, administering protocol and related study training, and evaluating site quality and integrity.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred.
  • Requires at least 2 years of on-site monitoring experience.
  • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
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