Clinical Research Associate, Sponsor Dedicated

Lifelancer
Any Location, MI
Category Healthcare
Job Description
Perform site monitoring visits, administer protocol and related study training, and ensure site compliance with study protocol, applicable regulations and guidelines, and sponsor requirements. Manage study progress and ensure quality of site practices.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • Requires at least 2 years of on-site monitoring experience
  • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements

Benefits

  • 401k Matching
  • Generous Paid Time Off
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