Clinical Research Associate - Sponsor Dedicated

Lifelancer
Overland Park, KS
Category Healthcare
Job Description
Perform monitoring and site management work to ensure that sites are conducting the study and reporting study data as required. Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, and data query generation and resolution.

Requirements

  • Bachelor's Degree in scientific discipline or health care
  • At least 1 year 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

  • Life insurance
  • 401(k) or other retirement plan
  • Health insurance
  • Disability insurance
  • Paid time off
  • Employee assistance program
  • Professional development opportunities
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