Clinical Research Associate, Sponsor Dedicated

Lifelancer
La Habra, CA
Category Consulting
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. Adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.

Requirements

  • Bachelor's Degree in scientific discipline or health care
  • 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
  • Written and verbal communication skills
  • Organizational and problem-solving skills
  • Effective time and financial management skills
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients

Benefits

  • 401k Matching
  • Health and welfare benefits
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