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Senior Clinical Research Coordinator
Job in
Columbus, Franklin County, Ohio, 43224, USA
Listed on 2026-02-22
Listing for:
Ohio State University
Full Time
position Listed on 2026-02-22
Job specializations:
-
Healthcare
Clinical Research
Job Description & How to Apply Below
Columbus Campus time type:
Full time posted on:
Posted Todayjob requisition :
R144929
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Job Title:
Senior Clinical Research Coordinator## Department:
Medicine | Clinical Trials Management Office Earnings
*
* Job Description:
** The Sr. CRC serves as lead resource in the execution of assigned clinical research studies in accordance with approved protocols administered by the non-cancer Center for Clinical Research Management (CCRM) for the Department of Dermatology; oversees, implements & coordinates conduct of daily activities of research studies; serves as primary reviewer of patient records to assess and identify patients who meet criteria for participation in research studies;
recruits, interviews and promotes study to eligible patients; educates patients and families of purpose, goals, and processes of clinical study; leads patient enrollment activities and ensures informed consent authorization is obtained & administered in compliance to regulatory & sponsor requirements; facilitates collection, processing & evaluation of biological samples, as well as scheduling and follow-through of patient care appointments, procedure
* s,* & other diagnostic testing; monitors patients for adverse reactions to study treatment, procedure or medication and notifies appropriate clinical professional to evaluate patient response, identify status of complications, & provide appropriate level of care; documents unfavorable responses and notifies research sponsors & applicable regulatory agencies; participates in collecting, extracting, coding, and analyzing clinical research data; assists with activities to ensure compliance with Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations;
participates in planning, organizing and preparing for external compliance and quality assurance and control reviews; actively participates in internal quality assurance audits; participates in development of new research protocols and contributes to planning of goals to meet study requirements; assists with preparation and submission of publications, research reports, and grant proposals.
** Minimum Education Required
** Bachelor’s Degree in biological sciences, health sciences or medical field or an equivalent combination of education and experience required.
** Minimum Experience Required
** Three years’ experience in a clinical research capacity conducting clinical research studies required. Clinical research certification from an accredited certifying agency is required (ACRP or SOCRA) and must be maintained.
Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen.
** Skills and Qualifications Desired/Preferred
** Four to six years of clinical research experience preferred; experience in a progressively responsible management capacity in a medical research environment preferred; experience or knowledge in neurological movement disorders preferred; computer skills required with experience using Microsoft Software applications desired.
* FUNCTION/SUBFUNCTION:
Research and…
Position Requirements
10+ Years
work experience
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