Clinical Research Associate - Sponsor Dedicated

Lifelancer
Carlsbad, 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. Conduct site visits, adapt and drive subject recruitment plans, administer protocol training, evaluate study site practices, and manage study progress.

Requirements

  • Bachelor's Degree in scientific discipline or health care
  • At least 1.5 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

Benefits

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