Clinical Research Associate, Sponsor Dedicated

Lifelancer
Panama City, FL
Category Healthcare
Job Description
Perform site monitoring visits and manage study sites to ensure compliance with study protocol and regulations. Requires on-site monitoring experience, good knowledge of clinical research regulatory requirements, and strong communication and organizational skills.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • At least 2 years of on-site monitoring experience
  • Good knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
  • Good therapeutic and protocol knowledge
  • Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint
  • Written and verbal communication skills including good command of English language
  • Organizational and problem-solving skills
  • Effective time and financial management skills
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