Clinical Research Coordinator Float-clinical Trials Management Office

The Ohio State University

Columbus, Ohio, USA
Coordinate clinical research activities
Assess patient records for eligibility
Recruit, interview, 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 assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients; obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements.
  • Supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors.

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, interview, and enroll patients
  • Obtain informed consent
  • Educate patients and families
  • Collect, process, and evaluate biological samples
  • Monitor patients for adverse reactions
  • Collect, extract, code, and analyze data
  • Ensure regulatory compliance

Nice-to-have

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

Key Requirements

  • Bachelor’s Degree or equivalent combination of education and experience
  • One year experience in a clinical research capacity
  • 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