Clinical Research Associate, Sponsor Dedicated

Lifelancer
Springfield, MA
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 to assigned sites
  • Evaluate the quality and integrity of study site practices
  • Manage the progress of assigned studies
  • Create and maintain appropriate documentation regarding site management
  • Collaborate and liaise with study team members
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