Sr. Clinical Research Associate, IQVIA

Lifelancer
Durham, NC
Category Healthcare
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.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred.
  • Requires at least 2 years of year 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.

Benefits

  • Generous Paid Time Off
  • 401k Matching
  • Health and Welfare Benefits
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