Clinical Research Coordinator Float-clinical Trials Management Office

The Ohio State University

Columbus, Ohio, US
Coordinate clinical research activities
Assess patient records for eligibility
Recruit and enroll patients
Coordinate and perform daily clinical research activities in accordance with approved protocols administered by the College of Medicine (COM) Center for Clinical Research Management (CCRM) in various COM Departments and Divisions conducting non-oncology human subjects research

Job Summary

  • Coordinate and perform daily clinical research activities in accordance with approved protocols administered by the College of Medicine (COM) Center for Clinical Research Management (CCRM) in various COM Departments and Divisions conducting non-oncology human subjects research.
  • Assists with monitoring patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of care.
  • Supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations.

Matching Summary

Coordinate and perform daily clinical research activities in accordance with approved protocols administered by the College of Medicine (COM) Center for Clinical Research Management (CCRM) in various COM Departments and Divisions conducting non-oncology human subjects research.

Skills & Requirements

Must-have

  • Coordinate clinical research activities
  • Assess patient records for eligibility
  • Recruit and enroll patients
  • Obtain informed consent
  • Educate patients and families
  • Collect and process biological samples
  • Monitor for adverse reactions
  • Extract and analyze clinical data

Nice-to-have

  • Knowledge of medical terminology
  • Experience with data base systems
  • Contribute to new research protocols

Key Requirements

  • Bachelor’s Degree or equivalent experience
  • One year clinical research experience
  • Computer experience required
  • Patient facing and required to be on site
  • Travel to various clinical research locations required

Work Rights

Not specified

Tailored Resume

Cover Letter