Clinical Research Associate, Sponsor Dedicated

Lifelancer
Any Location, NJ
Category Research
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
  • Ensure copies/originals of site documents are available
  • Create and maintain appropriate documentation regarding site management

Benefits

  • Health and welfare benefits
  • Other benefits
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