Clinical Research Coordinator (HS)

Job DescriptionClinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization for Division of Multiple Sclerosis (MS) specialty in the Department of Neurology; 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, amp; other diagnostic testing in accordance with study protocol; participates in the collection, processing amp; 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, amp; provide appropriate level of care; documents unfavorable responses and notifies research sponsors amp; 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 requirements.

Minimum Education Required:

Bachelor's Level Degree or equivalent combination of education and experience with a Major in social sciences or biological sciences.

Additional Education Desired:

Master's Degree with a Major in social sciences or biological sciences.

Required Qualifications:

Bachelor's degree in biological sciences, health sciences, social sciences, a related field or equivalent combination of education and experience required; one year experience in a clinical research capacity conducting clinical research studies required.

Desired Qualifications:

Clinical research certification from ACRP (Assn of Clinical Research Professionals) or SoCRA (Society of Clinical Research Assoc) desired; interest in working with neurological diseases/ disorders desired; experience with investigational drug trials and familiarity with OSU Research Foundation rules and regulations desired.

Requires successful completion of a background check. Selected candidate 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

This position is patient facing and therefore is required to be onsite.