Sr. Clinical Research Associate, IQVIA

Lifelancer
Bloomington, IN
Category Consulting
Job Description
Perform site monitoring visits, adapt, drive, and track subject recruitment plans, administer protocol and related study training, and evaluate site practices in accordance with contracted scope of work and Good Clinical Practice.

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) guidelines
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