Clinical Research Coordinator 2-Neurology
The Ohio State University Wexner Medical Center · Columbus, OH · Yesterday
AnalystFull-time
About the role
The Clinical Research Coordinator will 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.
Responsibilities
- Assesses 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
- Edits and educates patients and families of purpose, goals, and processes of clinical study
- Schedules and follows through with patient care appointments, procedures, & other diagnostic testing in accordance with study protocol
- Collects, processes & evaluates biological samples
- Administers, evaluates and calculates standardized scoring of diagnostic, psychological or behavioral testing or questionnaires
- Monitors 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
- Evaluates patients for compliance related to protocol
- Collects, extracts, codes, and analyzes 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
- Coordinates and prepares for external quality assurance and control reviews by IRB, federal or industry sponsors
- Participates in developing new research protocols and contributing to the 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
- Two to four 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)
Qualifications
- Minimum Education and Skills/Experience Required/Desired: Bachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required. Experience Required: One year experience in a clinical research capacity required. Desired Experience: Two to four years of relevant experience preferred.
- Desired Certification: Clinical research certification from an accredited certifying agency desired (ACRP or SOCRA).
- Requires successful completion of a background check.