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Clinical Senior Research Nurse
4 months ago
Functions as a Senior Research Nurse who will serves as primary resource in the execution of assigned clinical research studies in accordance with approved protocols administered by the non-cancer Clinical Trials Management Organization (CTMO) for the Department of Psychiatry; plans, implements amp; oversees daily conduct of protocol activities;; works closely with clinical research manager to assist with operational management of research unit including process improvement and clinical concerns. serves as lead providing mentorship to new and existing research staff through oversight of daily protocol activities; training programs and in-services; functions as central contact point for specialized disease specific protocols; reviews, evaluates and identifies patients eligible for participation in research studies; oversees and supports activities to recruit, interview and enroll study participants; plans, organizes and manages care of patients enrolled in research studies; develops and revises patient care orders; monitors delivery of patient care services and ensures proper and timely follow up; monitors and evaluates patient response to study treatments amp; medications to identify clinical complications; identifies, addresses, documents and reports adverse reactions to IRB and outside sponsors; educates and directs protocol compliance with physicians and staff nurses; serves as primary liaison with outside federal or industry sponsors; assists in developing tools to meet requirements of new protocols; manages protocols with increased clinical complexities including translational investigator-initiated research; assists in design and implementation of protocols; prepares research reports; assists in writing abstracts and manuscripts on research findings; attends and makes presentations at local and national meetings on research results; acts as a patient advocate by providing education to and responding to inquiries from patients about protocols; works with patients to ensure adherence with the protocol;
MINIMUM REQUIRED QUALIFICATIONS
Bachelor's degree in Nursing or equivalent combination of education and experience required. Requires clinical license or certification. Registered Nurse. 3 years of relevant experience required. 4-6 years of relevant experience preferred.
Oversight of data management and organization
Supervising/managing lab Research Assistants
Hiring and onboarding of new RAs
Time approvals
Oversight of studies from IRB approval to recruitment to close out.
Monitoring progress of all studies and ensuring there is movement within all of Dr. Coccaros studies.
Delegating tasks and serving as a means of communication between RAs and PI.
Point of contact when RAs need to elevate chain of command (specifically with study participants).
Overall Lab Coordinator - Point of contact for vendors, ordering, and invoice payments.
Oversight of upkeeping Environmental Health Safety standards and protocols for our medical lab.
