Research Data Associate

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 tomed.nyu.edu, and interact with us on LinkedIn, Glassdoor, Indeed, Facebook, XandInstagram.Position Summary:We have an exciting opportunity to join our team as a Research Data Associate. The research data associate is responsible for providing direct data and/or clinical research support of clinical trials, studies, and general research, under direct supervision. Works with clinical research center, CTSI, Beyond Bridges, and other medical center staff, including directors, managers, clinical information systems, research nursing, and regulatory services, and staff in other NYU Langone Health departments as needed. May also interface with patients and their families, community partners, and high school, undergraduate, and medical students and other clinical research center trainees. This role requires excellent communication and organizational skills, an understanding of medical research processes, and a genuine commitment to patient care and the communities we serve. The role is based at the NYULH Brooklyn Clinical Research Center with a multi-disciplinary research team that is dedicated to conducting clinical research in the community.Job Responsibilities: * Utilizes established quantitative and qualitative methodologies to collect patient, partner, staff, and/or trainee information for both research and evaluation project(s); gathers and compiles data, statistics, and other materials as needed. Inputs clinical and nonclinical data into the database and/or case report forms. Extracts data for publications or provides data collection from outside physicians offices. May perform library searches and retrieve reference materials from various sources and request articles from medical journals. * Ensures protocol compliance. Follows standard steps regarding eligibility criteria, follow-up process and documentation. * Compiles data and assists in consolidating and analyzing data for presentation to sponsoring and regulatory agencies. Reviews data with supervisor and then provides reports to all parties (eg, data and safety monitoring committee, the principal investigator, sponsoring agency, etc) on the progress of the study. * Recruits and screens potential patients/subjects for eligibility to the study. * Interacts with patient/subject and families in a courteous and professional manner. Collaborates with various personnel that may be involved with specific aspects in the study. * Demonstrates knowledge of policies and procedures of the host institution where the study is being conducted, including the regulatory requirements such as IRB and other approvals if necessary. * Initiates and continues regular contact with patients; encourages visit reminders and compliance to research; ensures contact with patients and their families is courteous, effective, professional, and cooperative. * Gathers, properly packages, stores, and transfers slides, samples, and other important materials. Coordinates the shipment and transfer of varied types of materials among the various departments and labs. * May complete assessments on study subjects/patients per protocol (with proper training); continue to follow through with items and patients as part of research study.Minimum Qu