Clinical Research Associate, Sponsor Dedicated

Lifelancer
Newark, NJ
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. The position requires a bachelor's degree in a scientific discipline or healthcare, at least 2 years of on-site monitoring experience, and good knowledge of clinical research regulatory 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
  • Create and maintain appropriate documentation regarding site management
  • Collaborate and liaise with study team members
  • Support development of project subject recruitment plan
  • Support site financial management

Benefits

  • Generous health and welfare and/or other benefits
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