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Clinical Research Coordinator

Buffalo, New York ~ November 07, 2018

Clinical Research Coordinator
The Clinical Research Associate I (Clinical Research Nurse Coordinator) performs a vital role for the Clinical Research Office (CRO) by coordinating various components of multiple clinical research studies at any time. This position reports to the CRO Associate Directors.
Primary responsibilities of the Clinical Research Nurse Coordinator include, but are not limited to:
Undertake coordinating tasks of clinical research studies.
Assist investigators in successful recruitment and retention of subjects.
Guide day-to-day operations of assigned studies, assuring adherence to protocol.
Generate accurate reports.
Resolve queries in a timely manner.
Maintain contact with Principal Investigator, monitoring agency, sponsor, and contracted vendors.
Generate IRB approved materials for distribution to study subjects to promote project enrollment and retention of enrolled subjects.
Oversee implementation of research studies, generation of qualitative and quantitative data and data collection forms and surveys.
Manage the day-to-day operations of the assigned project including development and implementation of research procedures and systems.
Assist Principal Investigator with administration of clinical trial protocols, including obtaining informed consents and screening subjects, maintaining research records and research subject records, managing correspondence, researching medical records, recording data, and attending training sessions.
Support the management of the CRO.

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