Sr. Clinical Research Associate, IQVIA

Lifelancer
Any Location, 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 and adapt, drive, and track subject recruitment plan in line with project needs.

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
  • Good therapeutic and protocol knowledge as provided in company training

Benefits

  • Incentive plans, bonuses, and/or other forms of compensation
  • Range of health and welfare and/or other benefits
]]>