Clinical Research Associate, Sponsor Dedicated

Lifelancer
Overland Park, KS
Category Research
Job Description
Perform site monitoring visits, adapt and drive subject recruitment plans, administer protocol and study training, and evaluate site practices to ensure proper conduct of the study protocol and applicable regulations. Manage study progress, track regulatory submissions and approvals, and ensure compliance with GCP and local regulatory requirements.

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
  • Therapeutic and protocol knowledge
  • Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint
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