Clinical Research Associate, Sponsor Dedicated

Lifelancer
Any Location, CA
Category Healthcare
Job Description
Perform site monitoring visits to ensure study compliance and report data as required by study protocol, regulations, and sponsor requirements. Adapt and drive subject recruitment plans, administer protocol training, and evaluate site practices. Manage study progress and create documentation for site management and monitoring visit findings.

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 Microsoft Office
  • Written and verbal communication skills
  • Organizational and problem-solving skills
  • Time and financial management skills
  • Ability to establish effective working relationships

Benefits

  • 401k Matching
  • Health and welfare benefits
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