Clinical Research Coordinator - Neurology

The Ohio State University

18h • Onsite

About The Position

Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the College of Medicine (COM) Center for Clinical Research Management (CCRM) the Department of Neurology/ Division of Neuromuscular Diseases, with a focus on Amyotrophic Lateral Sclerosis (ALS), or Lou Gehrig's disease; 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.
• Qualified candidates may be requested to complete a pre-employment physical, including a drug screen.

Nice To Haves

• Experience or knowledge in cognitive diseases/disorders 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

Responsibilities

• 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

Benefits

• Medical, dental and vision coverage, with Ohio State paying a significant portion of the cost.
• Paid time off, including sick and vacation time and 11 holidays.
• State retirement plan or an alternative retirement plan, both with generous employer contributions.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees