Clinical Research Coordinator 2-Neurology

The Ohio State University

3d • Onsite

About The Position

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 the Department of Neurology/ Division of Cognitive 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, & 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 requirements.

Requirements

• Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required.
• One year experience in a clinical research capacity required.
• Requires successful completion of a background check.
• This is a patient facing position and is required to be onsite.

Nice To Haves

• 2-4 years of relevant experience preferred.
• Experience or knowledge in cognitive diseases/disorders preferred.
• Knowledge of medical terminology desired.
• Computer skills required with experience using Microsoft Software applications desired.
• Clinical research certification from an accredited certifying agency desired (ACRP or SOCRA).
• Qualified candidates may be requested to complete a pre-employment physical, including a drug screen.

Responsibilities

• Coordinate and perform daily clinical research activities in accordance with approved protocols.
• Assess patient records to identify eligible participants.
• Recruit, interview, and enroll patients.
• Obtain informed consent and ensure compliance with regulatory and sponsor requirements.
• Educate patients and families about the study's purpose, goals, and processes.
• Coordinate patient care appointments, procedures, and diagnostic testing.
• Participate in the collection, processing, and evaluation of biological samples.
• Administer, evaluate, and calculate standardized scoring of diagnostic, psychological, or behavioral testing/questionnaires.
• Monitor patients for adverse reactions and notify appropriate clinical professionals.
• Document unfavorable responses and notify research sponsors and regulatory agencies.
• Evaluate patients for protocol compliance.
• Assist with collecting, extracting, coding, and analyzing clinical research data.
• Generate reports and review for data validity.
• Support activities to ensure compliance with IRB, FDA, federal, state, and industry sponsor regulations.
• Assist with coordinating and preparing for external quality assurance and control reviews.
• Participate in developing new research protocols and establishing study goals.

Benefits

• The university is an equal opportunity employer, including veterans and disability.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level