Clinical Research Associate, Sponsor Dedicated

Lifelancer
Kansas City, KS
Category Healthcare
Job Description
Perform site monitoring visits, manage site practices, track regulatory submissions and approvals, and collaborate with study team members.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • 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 Microsoft Word, Excel and PowerPoint
  • Written and verbal communication skills
  • Organizational and problem-solving skills
  • Effective time and financial management skills
  • Ability to establish and maintain effective working relationships
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