Clinical Research Associate, Sponsor Dedicated

Lifelancer
Any Location, NJ
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. Perform site monitoring visits, adapt and drive subject recruitment plan, administer protocol and related study training, and evaluate study site practices.

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
  • Good therapeutic and protocol knowledge
  • Computer skills, including 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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