Clinical Research Coordinator Float-clinical Trials Management Office

The Ohio State University

Columbus, Ohio, USA
On-site
Coordinate clinical research activities
Recruit and enroll patients
Obtain informed consent
Coordinate and perform daily clinical research activities in accordance with approved protocols

Job Summary

  • Coordinate and perform daily clinical research activities in accordance with approved protocols.
  • Assist with assessing patient records to identify eligible participants and recruit, interview, and enroll patients.
  • Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA, federal, state, and industry sponsor regulations.

Matching Summary

Coordinate and perform daily clinical research activities in accordance with approved protocols.

Skills & Requirements

Must-have

  • Coordinate clinical research activities
  • Recruit and enroll patients
  • Obtain informed consent
  • Collect and process biological samples
  • Administer diagnostic testing
  • Monitor patient adverse reactions
  • Collect and analyze clinical data
  • Ensure regulatory compliance

Nice-to-have

  • Knowledge of medical terminology
  • Experience with data base systems

Key Requirements

  • Bachelor's Degree or equivalent experience
  • One year clinical research experience
  • Computer experience required

Work Rights

Not specified

Tailored Resume

Cover Letter