As a Research Coordinator, you will coordinate the daily activities of the designated study or group of studies, coordinate and monitors research trials and actively oversee the recruitment of study participants. You will be asked to ensure that the study and study participants and clinicians adhere to Good Clinical Practice, and comply with regulatory and grant agency requirements, Further you will study protocol and maintain study records and collaborate with the Institutional Review Board, Clinical Trials Office, and sponsors as necessary.
Job Responsibilities Include:
Responsible for coordination of a designated study or group of studies. In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data. Keeps accurate and up-to-date records.
Collects, labels, logs, processes, data from subjects.
Schedules subjects for protocol-related evaluations. Collaborates with physicians, investigators and other healthcare providers. Promotes respect for subjects' rights.
Administers, scores and evaluates results of assessments as assigned and as related to study protocol. Collects data, confers with PI and forwards results to sponsor (internal or external).
Interfaces with the Office of Grants and Contracts (OGC) and Institutional Review Board (IRB) as necessary. Organizes all phases of grant process for submission to funding agencies as necessary.
Collaborates with PI and the Food and Drug Administration and drug companies on related issues. Adheres to Good Clinical Practice, and complies with regulatory and grant agency requirements. Follows protocol as developed. Keeps investigator or supervisor informed of developments.
Ensures availability of drug supplies and/or equipment for studies. Maintains drug accountability logs.
Liaisons with agencies including: IRB, OCG, pharmaceutical companies, laboratories, and equipment and supply companies, as needed.
Bachelor's Degree, preferably in a field of Science, Behavioral Science or related field, required.
Minimum of two (2) years progressively responsible related experience, required.
IRB Human Subject Protection training, prior to commencement of research, required.
Highly proficient in writing and communication skills.
Northern Westchester Hospital