Clinical Research Associate, Sponsor Dedicated

Lifelancer
Any Location, AZ
Category Research
Job Description
Perform site monitoring visits, administer protocol and related study training, evaluate site practices, and ensure quality and integrity of study site practices. Work with sites to adapt, drive, and track subject recruitment plan. Manage the progress of assigned studies, ensure copies/originals of site documents are available, and verify the Investigator's Site File is maintained in accordance with GCP and local regulatory requirements.

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

Benefits

  • 401k Matching
  • Retirement Plan
  • Generous Paid Time Off
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