Clinical Research Associate, Sponsor Dedicated

Lifelancer
Carlsbad, CA
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. Essential Functions include site monitoring visits, administering protocol and related study training, evaluating study site practices, and managing the progress of assigned studies.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • At least 2 years of year 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
  • Written and verbal communication skills
  • Organizational and problem-solving skills
  • Effective time and financial management skills
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