Sr. Clinical Research Associate, IQVIA

Lifelancer
Cleveland, OH
Category Healthcare
Job Description
Perform site monitoring visits, work with sites to adapt and track subject recruitment, administer protocol training, and manage study progress. Ensure quality and integrity of study site practices and maintain documentation.

Requirements

  • Bachelor's Degree in scientific discipline or health care
  • At least 2 years of on-site monitoring experience
  • Good knowledge of clinical research regulatory requirements and Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
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