Inside Higher Ed · 1 week ago
Clinical Research Coordinator - Surgery / Center for Clinical Research Management
Columbus, OH
Full-time
Onsite
Entry Level
1+ years expThe Ohio State University is a prominent educational institution, and they are seeking a Clinical Research Coordinator for their Center for Clinical Research Management. The role involves coordinating and performing clinical research activities, including patient recruitment and data management, while ensuring compliance with regulatory requirements.
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Responsibilities
Coordinate and perform daily clinical research activities in accordance with approved protocols
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
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
Qualification
Required
Bachelor's Level Degree or equivalent combination of education and experience with a Major in allied medicine professions or biological sciences
One year experience in a clinical research capacity conducting clinical research studies required
Preferred
Experience or knowledge in Neurosurgery 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
Company
Inside Higher Ed
Inside Higher Ed is the online source for news, opinion, and jobs related to higher education.
51-200 employees
Funding
Current Stage
Growth StageTotal Funding
unknown2022-01-10Acquired
2006-08-31Series Unknown
Leadership Team
Stephanie Shweiki
Director, Foundation Partnerships
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