The Ohio State University, Main Campus

Clinical Research Coordinator - Comprehensive Cancer Center

The Ohio State University, Main Campus

full-time

Posted on:

Origin:  • 🇺🇸 United States • Ohio

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Job Level

Junior

Tech Stack

Assembly

About the role

  • Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
  • Recruit, interview and enroll patients
  • Obtain informed consent and ensure consent process is administered in compliance with regulatory and sponsor requirements
  • Educate patients and families of purpose, goals, and processes of clinical study
  • Coordinate scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with the study protocol
  • Assist with monitoring patients for adverse reactions to study treatment, procedure, or medication and notifies appropriate clinical professionals to evaluate patient response, identify the status of complications, & provide the appropriate level of care
  • Document unfavorable responses and notify research sponsors & applicable regulatory agencies
  • Assist with collecting, extracting, coding, and analyzing clinical research data
  • Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state, and industry sponsor regulations
  • Assist with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors
  • Participate in activities to develop new research protocols and contributes to the establishment of study goals to meet protocol requirements

Requirements

  • Bachelor’s Degree in biological sciences, health sciences, social sciences, or other medical field or an equivalent combination of education and experience required.
  • One year of experience in a clinical research capacity is required .
  • Knowledge of medical terminology desired.
  • Clinical research certification from an accredited certifying agency desired.
  • Computer skills required with experience using Microsoft Office Software applications desired.
  • Must be able to effectively communicate, both face-to-face and in writing, with clinical staff, research participants, and outside collaborators.