Clinical Research Associate, Sponsor Dedicated

Lifelancer
Any Location, MD
Category Healthcare
Job Description
Perform site monitoring visits to ensure study compliance, adapt and drive subject recruitment plans, and manage study progress. Evaluate site practices and ensure adherence to regulations. Collaborate with study team members for project execution.

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
  • Good therapeutic and protocol knowledge
  • Computer skills, including Microsoft Word, Excel, and PowerPoint
  • Written and verbal communication skills
  • Organizational and problem-solving skills
  • Effective time and financial management skills

Benefits

  • 401k Matching
  • Health and welfare benefits
  • Bonuses
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