Ohio State University Wexner Medical Center
Clinical Research Coordinator
Ohio State University Wexner Medical Center, Columbus, Ohio, United States, 43224
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 the consent process is administered in compliance with regulatory and sponsor requirements. Educate patients and families about the purpose, goals, and processes of the clinical study. Coordinate scheduling and follow-up of patient care appointments, procedures, and other diagnostic testing in accordance with the study protocol. Assist with monitoring patients for adverse reactions to study treatments, procedures, or medications, and notify appropriate clinical professionals to evaluate patient response, identify complications, and provide appropriate care. Document adverse responses and notify research sponsors and 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 regulations, 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 developing new research protocols and contribute to establishing study goals to meet protocol requirements. Minimum Education Required
Bachelor's Degree in biological sciences, health sciences, social sciences, or related fields, or an equivalent combination of education and experience. Qualifications
One year of experience in a clinical research capacity involving human subjects is required. Knowledge of medical terminology is desired. Clinical research certification from an accredited agency is preferred. Computer skills, particularly with Microsoft Office applications, are required. Effective communication skills, both face-to-face and written, with clinical staff, research participants, and external collaborators, are essential. The OSUCCC James is the only cancer program in the United States featuring 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 nation's largest public universities.
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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 the consent process is administered in compliance with regulatory and sponsor requirements. Educate patients and families about the purpose, goals, and processes of the clinical study. Coordinate scheduling and follow-up of patient care appointments, procedures, and other diagnostic testing in accordance with the study protocol. Assist with monitoring patients for adverse reactions to study treatments, procedures, or medications, and notify appropriate clinical professionals to evaluate patient response, identify complications, and provide appropriate care. Document adverse responses and notify research sponsors and 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 regulations, 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 developing new research protocols and contribute to establishing study goals to meet protocol requirements. Minimum Education Required
Bachelor's Degree in biological sciences, health sciences, social sciences, or related fields, or an equivalent combination of education and experience. Qualifications
One year of experience in a clinical research capacity involving human subjects is required. Knowledge of medical terminology is desired. Clinical research certification from an accredited agency is preferred. Computer skills, particularly with Microsoft Office applications, are required. Effective communication skills, both face-to-face and written, with clinical staff, research participants, and external collaborators, are essential. The OSUCCC James is the only cancer program in the United States featuring 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 nation's largest public universities.
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