Sr. Clinical Research Associate, IQVIA

Lifelancer
Chicago, IL
Category Research
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. Perform site monitoring visits, adapt and drive subject recruitment plan, administer protocol and related study training, and evaluate site practices related to the proper conduct of the protocol and adherence to applicable regulations.

Requirements

  • Bachelor's Degree in scientific discipline or health care
  • 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
  • Good therapeutic and protocol knowledge

Benefits

  • Incentive plans
  • Bonuses
  • Health and welfare benefits
  • Other forms of compensation
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