Clinical Research Associate, Sponsor Dedicated

Lifelancer
Grand Junction, CO
Category Healthcare
Job Description
Perform site monitoring visits, adapt and drive subject recruitment plan, and manage study site practices to ensure quality and integrity. Manage study progress, track regulatory submissions and approvals, and generate and resolve data queries. Create and maintain documentation and collaborate with study team members.

Requirements

  • Bachelor's Degree in scientific discipline or health care
  • 2 years of on-site monitoring experience
  • Good knowledge of 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

Benefits

  • Health and welfare benefits
  • Incentive plans and bonuses
  • Other forms of compensation
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