Clinical Research Associate, Sponsor Dedicated

Lifelancer
Elk Grove, CA
Category Healthcare
Job Description
Perform site monitoring visits, adapt subject recruitment plan, administer protocol training, and evaluate study site practices to ensure adherence to regulations and sponsor requirements.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • At least 2 years of on-site monitoring experience
  • Good knowledge of clinical research regulatory requirements
  • Therapeutic and protocol knowledge
  • Computer skills including proficiency in Microsoft Office and mobile devices

Benefits

  • Generous Paid Time Off
  • 401k Matching
  • Retirement Plan
  • Health and welfare benefits
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