Sr. Clinical Research Associate, IQVIA

Lifelancer
Dallas, TX
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. Conduct site monitoring visits, adapt subject recruitment plans, and track project progress.

Requirements

  • Perform site monitoring visits
  • Work with sites to adapt subject recruitment plan
  • Administer protocol and related study training
  • Evaluate site practices
  • Manage study progress
  • Ensure site documentation is available

Benefits

  • 401k Matching
  • Health and Welfare Benefits
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