Clinical Research Coordinator - Oncology

Job Title Clinical Research Coordinator – Oncology Department CCC | Clinical Trials Office Position Summary 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. Working across multiple sites, the Coordinator supports protocols in various oncology specialties and is eligible for matching to new opportunities as they arise. Responsibilities Assist with assessing patient records to identify eligible participants for specified clinical research protocols. Pre‑screen and enroll patients, obtain informed consent in compliance with regulatory and sponsor requirements. Educate patients and families about study purpose, goals, and procedures. Coordinate scheduling and follow‑through of patient care appointments, procedures, and other diagnostic testing per the study protocol. Monitor patients for adverse reactions, report findings to appropriate clinical professionals, and document unfavorable responses for research sponsors and regulatory agencies. Collect, extract, and enter clinical research data with accuracy. Ensure compliance with Institutional Review Boards (IRB), FDA, federal, state, and sponsor regulations. Assist with preparing for internal and external audits and quality‑assurance reviews. Participate in development of new case report forms for Investigator‑Initiated Trials (IITs) and contribute to establishing study goals. Requirements Bachelor’s degree in biological sciences, health sciences, social sciences, or related field, or an equivalent combination of education and experience. At least one year of experience in a clinical research capacity involving human subjects. Knowledge of medical terminology preferred. Clinical research certification from an accredited agency desired. Proficiency with Microsoft Office (Word, Excel, Outlook) and electronic data capture tools. Strong verbal and written communication skills to engage clinical staff, research participants, and collaborators. Flexibility to travel between regional sites and adapt to operational needs. No sponsorship for work visas. Benefits and Development Full‑time, first shift schedule with a 40‑hour work week. Opportunities to pursue SoCRA or ACRP certification and engage in professional development programs. Tuition assistance for the Master of Clinical Research degree program through the College of Nursing. Annual Clinical Research Training Academy to deepen knowledge and career potential. Location James Cancer Hospital (0375), The Ohio State University Wexner Medical Center Position Type Regular Application Notes Final candidates are subject to a successful background check and may require a drug screen or physical examination. This position does not offer work‑visa sponsorship. Equal Opportunity Statement The university is an equal opportunity employer, including veterans and individuals with disabilities. #J-18808-Ljbffr