Clinical Research Associate, Sponsor Dedicated

Lifelancer
Gloucester, 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

  • Site monitoring visits
  • Administer protocol and related study training
  • Evaluate the quality and integrity of study site practices
  • Manage the progress of assigned studies

Benefits

  • Health and welfare benefits
  • Incentive plans, bonuses
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