Sr. Clinical Research Associate, IQVIA

Lifelancer
Overland Park, KS
Job Description
Perform site monitoring visits and manage site practices to ensure protocol compliance. Collaborate with study team members and manage study progress. Key responsibilities include administering protocol training, tracking regulatory submissions, and ensuring documentation is available.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • 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

Benefits

  • Potential base pay range $101,600 - $169,300
  • Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered
  • Range of health and welfare and/or other benefits
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