Clinical Research Coordinator (HS)

Details

Posted: 14-Mar-24

Type: Full-time

Salary: Open

Categories:

Healthcare
Staff/Administrative

Internal Number: R100534

Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the n on-cancer Clinical Trials Management Organization for in the Department of Neurology/Division of Cognitive Medicine; identifies and assesses eligibility of patients for consideration of participation in clinical research studies; recruits, interviews and enrolls patients into clinical studies; obtains informed consent; coordinates and documents care of patients; ensures proper follow-up visits are scheduled and conducted in accordance with protocol; prepares study materials; provides physician with study mandated criteria necessary for patient orders, response, complications, and to ensure protocol compliance; coordinates care of patients on clinical research protocols to include evaluation and analysis of research data; collects and enters all data for all patients enrolled on protocol; communicates with clinical research team, research manager, and outside federal or industry sponsor regarding protocol and patient status when applicable; participates in ensuring protocol compliance with all federal sponsor and industry regulations; assists in developing plans to meet requirements of new protocols; participates in implementation process; assists physician to assess patient reaction to any modifications or treatment that are part of protocol; reports and documents adverse reactions to clinical research team and research manager; assists in preparation of research presentations and papers for publication; assists in preparation of grants for future funded proposals; communicates with clinical research team, research manager, IRB and outside sponsors when applicable regarding adverse reactions; educates patients and their families of purpose, processes and goals of clinical study; answers questions regarding research protocols; participates in evaluating patients for compliance related to protocol.

MINIMUM REQUIRED QUALIFICATIONS
Bachelors Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience required. 1 year of relevant experience required. 2-4 years of relevant experience preferred.

Create a Job Alert for Similar Jobs
Logo
About The Ohio State University
The Ohio State University is a dynamic community of diverse resources, where opportunity thrives and where individuals transform themselves and the world. Founded in 1870, Ohio State is a world-class public research university and the leading comprehensive teaching and research institution in the state of Ohio. With more than 63,000 students (including 57,000 in Columbus), the Wexner Medical Center, 14 colleges, 80 centers and 175 majors, the university offers its students tremendous breadth and depth of opportunity in the liberal arts, the sciences and the professions.
Connections working at The Ohio State University
More Jobs from This Employer
https://main.hercjobs.org/jobs/19873337/clinical-research-coordinator-hs
Return to Search Results