More jobs:
Clinical Research Coordinator; HS
Job in
Columbus, Franklin County, Ohio, 43224, USA
Listed on 2026-01-02
Listing for:
Ohio State University
Full Time
position Listed on 2026-01-02
Job specializations:
-
Healthcare
Clinical Research
Job Description & How to Apply Below
Clinical Research Coordinator (HS) page is loaded## Clinical Research Coordinator (HS) locations:
Columbus Campus time type:
Full time posted on:
Posted Todayjob requisition :
R141157
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Job Title:
Clinical Research Coordinator (HS)## Department:
Medicine | IM Pulmonary Critical Care and Sleep
** Job Description
** Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer College of Medicine (COM) Center for Clinical Research Management (CCRM) for Pulmonary/Sleep/Critical Care Division in the Department of Internal Medicine; assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols; recruits, interviews and enrolls patients;
obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements; educates patients and families of purpose, goals, and processes of clinical study; coordinates scheduling and follow-through of patient care appointments, procedures, & other diagnostic testing in accordance with study protocol; participates in the collection, processing & evaluation of biological samples; administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires;
assists with monitoring 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 evaluating patients for compliance related to protocol; assists with collecting, extracting, coding, and analyzing clinical research data;
generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors; participates in activities to develop new research protocols and contributes to establishment of study goals to meet protocol.
** Minimum Education Required
** Bachelor's Level Degree or equivalent combination of education and experience with a Major in biological sciences
** Required Qualifications
** Bachelor's Degree in biological sciences, health sciences or other medical field or an equivalent combination of education and experience required; one year experience in a clinical research capacity required;
** Desired Qualifications
** Experience or knowledge in diseases of the lungs preferred; knowledge of medical terminology desired; clinical research certification from an accredited certifying agency desired; computer skills required with experience using Microsoft Software applications desired.
Requires successful completion of a background check. Qualified candidates may be requested to complete a pre-employment physical, including a drug screen.
* FUNCTION/SUBFUNCTION:
Research and Scholarship/Clinical Research
** CAREER BAND:
Individual Contributor
- Specialized
*
* CAREER LEVEL:
S2*## Additional Information:
This is a patient facing position and is required to be in the office.##
Location:
Blankenship Hall (0360)## Position Type:
Regular## Scheduled
Hours:
40##
** Shift:
** First Shift
*** Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.
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