Clinical Research Associate, Sponsor Dedicated

Lifelancer
Any Location, NY
Category Research
Job Description
Perform site monitoring visits, administer protocol and related study training, and manage study progress by tracking regulatory submissions and approvals, recruitment and enrollment, and data query generation and resolution.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • 2 years of on-site monitoring experience
  • Good knowledge of clinical research regulatory requirements
  • Therapeutic and protocol knowledge
  • Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint
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