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Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by thenon-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.
Full Time
Hospital
$80k-104k (estimate)
11/04/2023
03/31/2024
wexnermedical.osu.edu
COLUMBUS, OH
15,000 - 50,000
1834
Private
MICHAEL V DRAKE
$3B - $5B
Hospital
The job skills required for Clinical Research Coordinator (HS) include Clinical Research, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Research Coordinator (HS). That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Research Coordinator (HS). Select any job title you are interested in and start to search job requirements.
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