Clinical Research Associate, Sponsor Dedicated

Lifelancer
Any Location, CA
Category Healthcare
Job Description
Perform site monitoring visits, work with sites to adapt and track subject recruitment plan, administer protocol and related study training, and evaluate the quality and integrity of study site practices.

Requirements

  • Bachelor's Degree in scientific discipline or health care
  • At least 2 years of on-site monitoring experience
  • Good knowledge of clinical research regulatory requirements
  • Good therapeutic and protocol knowledge
  • Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint
  • Written and verbal communication skills
  • Organizational and problem-solving skills
  • Effective time and financial management skills

Benefits

  • Generous Paid Time Off
  • 401k Matching
  • Retirement Plan
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