The Ohio State University
Clinical Research Coordinator (HS)
The Ohio State University, Detroit, Michigan, United States, 48228
Clinical Research Coordinator (HS)
Department: Medicine | Family Medicine – Family Medicine Northwest (2580) – First Shift, 40 hours per week – Regular Scheduled Hours
Location:
Family Medicine Northwest (2580); Shift: First Shift
Job Title:
Clinical Research Coordinator – coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non‑cancer Center for Clinical Research Management for the Department of Family Medicine.
Responsibilities:
Recruit, interview and enroll patients; obtain informed consent in compliance with regulatory and sponsor requirements.
Educate patients and families about the purpose, goals and processes of clinical studies; coordinate scheduling and follow‑through of patient care appointments, procedures and diagnostic testing in accordance with study protocols.
Collect, process and evaluate biological samples; administer and evaluate standardized scoring of diagnostic, psychological or behavioral testing or questionnaires.
Assist with monitoring patients for adverse reactions to study treatment, procedure or medication and notify appropriate clinical professional to evaluate patient response and provide appropriate level of care.
Document adverse responses and notify research sponsors and applicable regulatory agencies; assist with collecting, coding, extracting and analyzing clinical research data; generate reports and review data to ensure validity of data.
Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA, federal, state and industry sponsor regulations; coordinate and prepare for external quality assurance and control reviews by IRB, federal or industry sponsors.
Participate in activities to develop new research protocols and contribute to establishment of study goals to meet protocol requirements.
Minimum Education Required
Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience.
Minimum Experience Required
One year experience in a clinical research capacity.
Experience and/or Skills Desired
Experience or knowledge in Family Medicine and chronic diseases 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.
The university is an equal opportunity employer, including veterans and disability.
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Location:
Family Medicine Northwest (2580); Shift: First Shift
Job Title:
Clinical Research Coordinator – coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non‑cancer Center for Clinical Research Management for the Department of Family Medicine.
Responsibilities:
Recruit, interview and enroll patients; obtain informed consent in compliance with regulatory and sponsor requirements.
Educate patients and families about the purpose, goals and processes of clinical studies; coordinate scheduling and follow‑through of patient care appointments, procedures and diagnostic testing in accordance with study protocols.
Collect, process and evaluate biological samples; administer and evaluate standardized scoring of diagnostic, psychological or behavioral testing or questionnaires.
Assist with monitoring patients for adverse reactions to study treatment, procedure or medication and notify appropriate clinical professional to evaluate patient response and provide appropriate level of care.
Document adverse responses and notify research sponsors and applicable regulatory agencies; assist with collecting, coding, extracting and analyzing clinical research data; generate reports and review data to ensure validity of data.
Support activities to ensure compliance with all Institutional Review Boards (IRB), FDA, federal, state and industry sponsor regulations; coordinate and prepare for external quality assurance and control reviews by IRB, federal or industry sponsors.
Participate in activities to develop new research protocols and contribute to establishment of study goals to meet protocol requirements.
Minimum Education Required
Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience.
Minimum Experience Required
One year experience in a clinical research capacity.
Experience and/or Skills Desired
Experience or knowledge in Family Medicine and chronic diseases 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.
The university is an equal opportunity employer, including veterans and disability.
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