Clinical Research Associate, Sponsor Dedicated

Lifelancer
Overland Park, KS
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

  • Perform site monitoring visits
  • Administer protocol and related study training
  • Evaluate the quality and integrity of study site practices
  • Manage the progress of assigned studies
  • Ensure copies/originals site documents are available for filing in the Trial Master File (TMF)
  • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans
  • Collaborate and liaise with study team members

Benefits

  • 401k Matching
  • Health and Welfare Benefits
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