Clinical Research Associate, Sponsor Dedicated

Lifelancer
Any Location, MN
Category Research
Job Description
Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Conduct site monitoring visits, adapt and drive subject recruitment plans, and establish regular communication with sites.

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
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint

Benefits

  • Health and welfare benefits
  • Bonus plans
  • Incentive plans
]]>