Inside Higher Ed
Clinical Research Coordinator (HS)
Department: Family Medicine | Ohio State University, Columbus, OH
Job Overview Coordinate and perform daily clinical research activities in Family Medicine as part of the Center for Clinical Research Management.
Responsibilities
Assess patient records to identify eligible participants for clinical research protocols.
Recruit, interview, enroll patients and obtain informed consent in compliance with regulatory and sponsor requirements.
Educate patients and families on study purpose, goals, and processes.
Coordinate scheduling, follow‑through of patient care appointments, procedures, and diagnostic testing per protocol.
Collect, process, and evaluate biological samples and administer standardized scoring of diagnostic or behavioral testing.
Monitor patients for adverse reactions, document responses, and notify sponsors and regulatory agencies.
Assist with monitoring compliance related to protocol and collect, extract, code, and analyze clinical research data.
Generate reports, review data validity, and support compliance with IRB, FDA, and sponsor regulations.
Participate in external quality assurance reviews and development of new research protocols.
Qualifications
Bachelor’s degree in biological, health, social sciences or equivalent combination of education and experience.
One year of clinical research experience.
Knowledge of Family Medicine, chronic diseases and medical terminology preferred.
Clinical research certification (accredited) desirable.
Proficient computer skills, especially Microsoft Office.
Successful completion of a background check, and possible pre‑employment physical including drug screen.
Additional Information
Location: Family Medicine Northwest (2580)
Position type: Regular
Scheduled hours: 40 per week
Shift: First Shift
Employment level: Individual Contributor – Specialized
We are an equal‑opportunity employer. The university complies with Ohio Revised Code §3345.0216 and supports a community dedicated to equity and inclusion.
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Job Overview Coordinate and perform daily clinical research activities in Family Medicine as part of the Center for Clinical Research Management.
Responsibilities
Assess patient records to identify eligible participants for clinical research protocols.
Recruit, interview, enroll patients and obtain informed consent in compliance with regulatory and sponsor requirements.
Educate patients and families on study purpose, goals, and processes.
Coordinate scheduling, follow‑through of patient care appointments, procedures, and diagnostic testing per protocol.
Collect, process, and evaluate biological samples and administer standardized scoring of diagnostic or behavioral testing.
Monitor patients for adverse reactions, document responses, and notify sponsors and regulatory agencies.
Assist with monitoring compliance related to protocol and collect, extract, code, and analyze clinical research data.
Generate reports, review data validity, and support compliance with IRB, FDA, and sponsor regulations.
Participate in external quality assurance reviews and development of new research protocols.
Qualifications
Bachelor’s degree in biological, health, social sciences or equivalent combination of education and experience.
One year of clinical research experience.
Knowledge of Family Medicine, chronic diseases and medical terminology preferred.
Clinical research certification (accredited) desirable.
Proficient computer skills, especially Microsoft Office.
Successful completion of a background check, and possible pre‑employment physical including drug screen.
Additional Information
Location: Family Medicine Northwest (2580)
Position type: Regular
Scheduled hours: 40 per week
Shift: First Shift
Employment level: Individual Contributor – Specialized
We are an equal‑opportunity employer. The university complies with Ohio Revised Code §3345.0216 and supports a community dedicated to equity and inclusion.
#J-18808-Ljbffr