The Ohio State University's Department of Internal Medicine/Division of Benign Hematology is seeking a Clinical Research Coordinator to manage and execute daily clinical research activities for their non-cancer Center for Clinical Research Management.
Requirements
- assists with assessing patient records to identify patients who are eligible to participate in specified clinical research protocols
- obtains informed consent and ensures consent process is administered in compliance to regulatory and sponsor requirements
- 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
- assists with collecting, extracting, coding, and analyzing clinical research data
Responsibilities
- coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer Center for Clinical Research Management for the Department of Internal Medicine/Division of Benign Hematology
- 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
- 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
- assists with collecting, extracting, coding, and analyzing clinical research data
Other
- 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.
- Experience or knowledge in sickle cell or hemophilia and chronic diseases preferred
- knowledge of medical terminology desired
- clinical research certification from an accredited certifying agency desired
