Clinical Research Associate, Sponsor Dedicated

Lifelancer
Any Location, CA
Category Healthcare
Job Description
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Monitor and track subject recruitment, case report form completion and submission, and data query generation and resolution.

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
  • Good therapeutic and protocol knowledge
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint

Benefits

  • Medical, Dental, and Vision
  • Paid Time Off (vacation, sick leave, holidays)
  • 401(k) Savings Plan
  • Disability Benefits
  • Employee Assistance Program
  • Life Insurance
  • Paid Family Leave
  • Retirement Plan
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