Sr. Clinical Research Associate, IQVIA

Lifelancer
Franklin, TN
Category Research
Job Description
Perform site monitoring visits, administer protocol and related study training, and evaluate the quality and integrity of study site practices. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form completion and submission, and data query generation and resolution.

Requirements

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

Benefits

  • 401k Matching
  • Retirement Plan
  • Health and welfare benefits
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