The Ohio State University Wexner Medical Center
Clinical Research Coordinator
The Ohio State University Wexner Medical Center, Columbus, Ohio, United States, 43224
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Clinical Research Coordinator
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The Ohio State University Wexner Medical Center . Current Employees and Students: Please log in to Workday to use the internal job search and application process. Overview
The Clinical Research Coordinator coordinates and performs daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for the Department of Emergency Medicine. The role assists with assessing patient records to identify eligible patients, recruits, interviews and enrolls participants, obtains informed consent, and ensures the consent process complies with regulatory and sponsor requirements. The coordinator educates patients and families about the purpose, goals, and processes of the clinical study; coordinates scheduling and follow-through of visits, procedures, and other diagnostic testing in accordance with the study protocol. The role may involve participation in the collection, processing and evaluation of biological samples, administering questionnaires, monitoring patients for adverse reactions, and notifying appropriate clinical professionals as needed. The coordinator also contributes to data collection, extraction, coding, and analysis, generates reports, and assists with ensuring data validity and regulatory compliance with IRB, FDA, and sponsor requirements. This includes coordinating for external quality assurance and control reviews and contributing to the development of new research protocols to meet study goals. Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review the frequently asked questions. Final candidates are subject to successful completion of a background check; a drug screen or physical may be required during the post-offer process. The university is an equal opportunity employer, including veterans and disability. Responsibilities
Coordinate and perform daily clinical research activities in accordance with approved protocols. Assess patient records to identify eligibility for specified clinical research protocols; recruit, interview, and enroll patients; obtain informed consent and ensure consent process compliance with regulatory and sponsor requirements. Educate patients and families about the purpose, goals, and processes of the clinical study; coordinate scheduling and follow-through of patient care appointments, procedures, and diagnostic testing. Participate in the collection, processing, and evaluation of biological samples; administer questionnaires; monitor patients for adverse reactions; notify appropriate clinical professionals to evaluate patient response and provide appropriate care. Document unfavorable responses and notify research sponsors and applicable regulatory agencies; assess patient compliance with the protocol. Assist with collecting, extracting, coding, and analyzing clinical research data; generate reports and reviews to ensure data validity. Support activities to ensure compliance with IRB, FDA, and federal/state sponsor regulations; assist with coordinating external quality assurance and control reviews. Participate in activities to develop new research protocols and contribute to establishing study goals to meet protocol requirements. Qualifications
Seniority level: Entry level Employment type: Full-time Job function: Research, Analyst, and Information Technology Industry: Hospitals and Health Care Additional information
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Clinical Research Coordinator
role at
The Ohio State University Wexner Medical Center . Current Employees and Students: Please log in to Workday to use the internal job search and application process. Overview
The Clinical Research Coordinator coordinates and performs daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for the Department of Emergency Medicine. The role assists with assessing patient records to identify eligible patients, recruits, interviews and enrolls participants, obtains informed consent, and ensures the consent process complies with regulatory and sponsor requirements. The coordinator educates patients and families about the purpose, goals, and processes of the clinical study; coordinates scheduling and follow-through of visits, procedures, and other diagnostic testing in accordance with the study protocol. The role may involve participation in the collection, processing and evaluation of biological samples, administering questionnaires, monitoring patients for adverse reactions, and notifying appropriate clinical professionals as needed. The coordinator also contributes to data collection, extraction, coding, and analysis, generates reports, and assists with ensuring data validity and regulatory compliance with IRB, FDA, and sponsor requirements. This includes coordinating for external quality assurance and control reviews and contributing to the development of new research protocols to meet study goals. Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review the frequently asked questions. Final candidates are subject to successful completion of a background check; a drug screen or physical may be required during the post-offer process. The university is an equal opportunity employer, including veterans and disability. Responsibilities
Coordinate and perform daily clinical research activities in accordance with approved protocols. Assess patient records to identify eligibility for specified clinical research protocols; recruit, interview, and enroll patients; obtain informed consent and ensure consent process compliance with regulatory and sponsor requirements. Educate patients and families about the purpose, goals, and processes of the clinical study; coordinate scheduling and follow-through of patient care appointments, procedures, and diagnostic testing. Participate in the collection, processing, and evaluation of biological samples; administer questionnaires; monitor patients for adverse reactions; notify appropriate clinical professionals to evaluate patient response and provide appropriate care. Document unfavorable responses and notify research sponsors and applicable regulatory agencies; assess patient compliance with the protocol. Assist with collecting, extracting, coding, and analyzing clinical research data; generate reports and reviews to ensure data validity. Support activities to ensure compliance with IRB, FDA, and federal/state sponsor regulations; assist with coordinating external quality assurance and control reviews. Participate in activities to develop new research protocols and contribute to establishing study goals to meet protocol requirements. Qualifications
Seniority level: Entry level Employment type: Full-time Job function: Research, Analyst, and Information Technology Industry: Hospitals and Health Care Additional information
We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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