Clinical Research Coordinator - CCC | Clinical Trials Office

Ohio State University

Hamilton, OHFull-timePosted Apr 30, 2026

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Qualifications

  • •Bachelor’s Degree in biological sciences, health sciences, social sciences, or other related field, or an equivalent combination of education and experience required
  • •One year of experience in a clinical research capacity (human subjects) is required;
  • •Must be able to effectively communicate, both face-to-face and in writing, with clinical staff, research participants, and outside collaborators

Responsibilities

  • •The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered by the Clinical Trials Office (CTO) within the Comprehensive Cancer Center at The Ohio State University Wexner Medical Center
  • •Assist with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
  • •Identify, pre-screen 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, and entering 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 internal and external audits and quality assurance reviews by IRB, federal or industry sponsors
  • •Participate in activities to develop new case report forms for Investigator Initiated Trials (IITs) and contribute to the establishment of study goals to meet protocol requirements
  • •9 more items(s)
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