To oversee several research studies and perform all aspects of patient contact related to that study (i.e., recruiting, scheduling, performing all patient tests and completing all documentation as outlined by the protocol and required by the Internal Medicine Research Center SOP’s). This includes phlebotomy and processing of specimens, ECG’s, and vital signs. To work with the clinical research team on various other clinical study protocols as needed, including recruitment and study data collection.
*This position is Co-Terminus Funded, position will end when the study concludes.
Responsibilities:
Assist with planning and preparing all details necessary for smooth operation of a study prior to study initiation.
Evaluate potential study volunteers on an individual basis and obtain in-depth medical histories as related to study inclusion/exclusion criteria to assist the investigator in the eligibility evaluations for enrollment of a potential patient. Schedule patients for all study visits according to the schedule required by the study protocol.
Review study protocols, informed consent forms, and follow-up procedures with potential study patients.
Screen and recruit patients through chart reviews, phone calls, attendance at lectures, health fairs, etc., as well as to coordinate the recruitment efforts of other clinical research staff.
Collect and document all data required by the study protocols and maintain the subject binders in an organized manner. Maintain and organize all regulatory documents to be readily accessible for study monitors.
Assist with performing various patient tests as needed, including phlebotomy and vital signs, processing and shipping of specimens. Ensure appropriate specimen collection as indicated by the study protocol. Review laboratory data and communicate abnormal values to the principal investigator and the primary care provider.
Transcribe study data from charts onto the case report forms, if required. Perform database entry and assist with data in electronic data capture (EDC) systems.
Assess and document subject compliance with medications and visits.
Coordinate the activities of various research team members to ensure completion of study objectives.
Responsible for notifying proper personnel when required supplies are needed.
Qualifications:
Preferred:
Bachelor’s degree in Biology, Chemistry or another field related to the specific field of research from a four-year college or university.
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