Research Coordinator

NYU Grossman School of Medicine • New York, NY • 2h ago

NYU Grossman School of Medicine is one of the nation's top-ranked medical schools. For 175 years, NYU Grossman School of Medicine has trained thousands of physicians and scientists who have helped to shape the course of medical history and enrich the lives of countless people. An integral part of NYU Langone Health, the Grossman School of Medicine at its core is committed to improving the human condition through medical education, scientific research, and direct patient care. At NYU Langone Health, equity and inclusion are fundamental values. We strive to be a place where our exceptionally talented faculty, staff, and students of all identities can thrive. We embrace inclusion and individual skills, ideas, and knowledge.For more information, go to med.nyu.edu, and interact with us on LinkedIn, Glassdoor, Indeed, Facebook, Twitter and Instagram.Position Summary:We have an exciting opportunity to join our team as a Research Coordinator.The Research Coordinator will support the Protocol Development and Monitoring Unit, in some PRMS activities, and protocol development. The Research Coordinator is responsible for generating progress monitoring reports of PRMC related activities for cancer clinical research studies conducted at the Laura and Isaac Perlmutter Cancer Center.Job Responsibilities: Demonstrates knowledge of the organizations Core Values and incorporates them into the performance of duties. In conjunction with investigators, develops and reviews all PCC Investigator Initiated trials ensuring compliance with institutional and regulatory body policies, guidances and regulation and IRB approval requirements. Create and maintain internal database content of all cancer related trial status and accrual information. Develops an advanced competency of Good Clinical Practice (GCP) guidelines, Federal Regulations that govern the conduct of human subjects research as well as Institutional Review Board and institutional policies and procedures related to human subjects research. Develops an intermediate competency of medical terminology in the oncology field. Navigates and understands how to extract information from the protocol in order to create and maintain content for the NYULH Cancer clinical trials website. Maintains files in an organized and up-to-date manner in order to facilitate their retrieval and maintains copies of all required on-going documentation and forms for the files. Responsible for logging trials into the Clinical Research Management System. Ensure data is complete and correct prior to review. Provides coverage to PRMC Coordinator as advised by Program Manager. Participates in special projects and performs other duties as required. Demonstrates knowledge of the organizations Core Values and incorporates them into the performance of duties. In conjunction with investigators, develops and reviews all PCC Investigator Initiated trials ensuring compliance with institutional and regulatory body policies, guidances and regulation and IRB approval requirements. Create and maintain internal database content of all cancer related trial status and accrual information. Develops an advanced competency of Good Clinical Practice (GCP) guidelines, Federal Regulations that govern the conduct of human subjects research as well as Institutional Review Board and institutional policies and procedures related to human subjects research. Develops an intermediate competency of medical terminology in the oncology field. Navigates and understands how to extract information from the protocol in order to create and maintain content for the NYULH Cancer clinical trials website. Maintains files in an organized and up-to-date manner in order to facilitate their retrieval and maintains copies of all required on-going documentation and forms for the files. Responsible for logging trials into the Clinical Research Management System. Ensure data is complete and correct p

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