Clinical Research Associate, Sponsor Dedicated

Lifelancer
Portland, ME
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. Key responsibilities include site monitoring visits, adapting and driving subject recruitment plans, and managing study progress.

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
  • Therapeutic and protocol knowledge
  • Computer skills including Microsoft Office and use of a laptop and mobile devices
  • Written and verbal communication skills
  • Organizational and problem-solving skills
  • Time and financial management skills
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