What are the responsibilities and job description for the Clinical Research Coordinator, CCC | Clinical Trials Office position at Ohio State University Wexner Medical Center?
Job Description
The Clinical Research Coordinator performs daily clinical research activities in accordance with approved protocols administered by the Clinical Trials Office within the Comprehensive Cancer Center at The Ohio State University Wexner Medical Center.
Responsibilities
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, amp; 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, amp; provide the appropriate level of care
Document unfavorable responses and notify research sponsors amp; 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
Minimum Education Required
Bachelors Degree in biological sciences, health sciences, social sciences, or other medical field or an equivalent combination of education and experience required.
Required Qualifications
One year of experience in a clinical research capacity (human subjects) 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.
The OSUCCC James is the only cancer program in the United States that features a National Cancer Institute (NCI)-designated comprehensive cancer center aligned with a nationally ranked academic medical center and a freestanding cancer hospital on the campus of one of the nations largest public universities.
Research and Scholarship Clinical Research Individual Contributor / Specialized S2
