Clinical Research Associate, Sponsor Dedicated, IQVIA

Lifelancer
Durham, NC
Category Healthcare
Job Description
Perform site monitoring visits and ensure sites are conducting studies as required by the study protocol, applicable regulations and guidelines, and sponsor requirements. Ideal candidates will have 1-2 years of onsite monitoring experience with expertise in Cardiovascular/Renal/Metabolic, Oncology, and/or Neurology.

Requirements

  • Bachelor's Degree in scientific discipline or health care
  • Basic knowledge of, and skill in applying, applicable clinical research regulatory requirements
  • Good therapeutic and protocol knowledge
  • 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

  • Medical, dental, and vision insurance
  • 401(k) and/or other retirement plan
  • Paid time off and holidays
  • Professional development opportunities
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