Clinical Research Associate, Sponsor Dedicated

Lifelancer
City of Rochester, NY
Category Healthcare
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 evaluate the quality and integrity of study site practices.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred.
  • Requires at least 2 years of year of on-site monitoring experience.
  • Good knowledge of, and skill in applying, applicable clinical research regulatory requirements.
  • Good therapeutic and protocol knowledge as provided in company training.
  • Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint and use of a laptop computer and iPhone and iPad (where applicable).
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