Sr. Clinical Research Associate, IQVIA

Lifelancer
Chicago, IL
Category Operations
Job Description
Perform site monitoring visits, work with sites to adapt and track subject recruitment plan, 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 preferred.
  • At least 2 years of on-site monitoring experience.
  • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
  • Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
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