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Clinical Research Regulatory Coordinator

South Jordan, United States

Regulatory Coordinator

Full Time - Non Exempt

JOB SUMMARY: This position is responsible for the regulatory process and management in compliance with Standard Operation Procedures (SOP’s) and Good Clinical Practice (GCP) associated with the UCS clinical research program consisting of multiple studies at central and satellite sites in partnership with pharmaceutical companies.

Knowledge, Skills, and Abilities:

The incumbent must possess exceptional organizational capacity, high attention to detail, and outstanding communication skills which are critical to the position and are considered mandatory.

Excellent oral and written communication and time management skills are required with the ability to function independently. Must be able to prioritize workload, and establish systems needed to achieve specific regulatory goals.

Education

High School education or equivalent required, BS in a health-related field preferred. Incumbent must have clinical research experience with a minimum of 6+ years of regulatory experience. Excellent computer literacy (experience with Excel and Microsoft Word).

AA/EOE

Job Type: Full-time

Benefits:

  • 401(k)
  • 401(k) matching
  • Dental insurance
  • Employee assistance program
  • Flexible spending account
  • Health insurance
  • Health savings account
  • Life insurance
  • Paid time off
  • Retirement plan
  • Tuition reimbursement

Work Location: In person

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