Clinical Research Associate, Sponsor Dedicated

Lifelancer
Redondo Beach, 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 performing site monitoring visits, adapting and driving subject recruitment plan, administering protocol and related study training, evaluating study site practices, managing study progress, and creating and maintaining documentation.

Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • At least 2 years 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
  • Written and verbal communication skills including good command of English language
  • 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

  • Generous Paid Time Off
  • 401k Matching
  • Retirement Plan
  • Health and Welfare Benefits
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