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Research Coordinator

NYU Grossman School of Medicine

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At a glance

Compensation
No compensation found
Location
NEW YORK, NY
Work Authorization
Not specified

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Job overview

The Research Coordinator supports studies in the Division of Cardiology’s prevention center and cardio-rheumatology program. The role assists with recruitment, enrollment, data collection, and study coordination; conducts informed consent and study visits; and helps ensure protocols are followed in accordance with Good Clinical Practices and HIPAA. The coordinator also works with patients, investigators, research teams, sponsors, and medical-center collaborators.

Skills & qualifications

RequiredNice to have

Skills

Research Study CoordinationParticipant RecruitmentParticipant EnrollmentResearch Data CollectionInformed ConsentRegulatory ComplianceData ManagementData AnalysisIntraoperative Monitoring

Full job description

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 Coordinator. Responsible for providing moderate to advanced range of coordination of research studies conducted within the Division of Cardiologys prevention center and cardio-rheumatology program. Coordinator will assist with the recruitment, enrollment, research data collection and study coordination activities. Performs intra-operative monitoring and serves as liaison with internal and external funding agencies. Ensures the accurate execution of research protocols in accordance with Good Clinical Practices, HIPAA, and required obligations to patient/subject, Principal Investigator, Research Team and sponsor. Interfaces directly with patients/subjects, Principal Investigator, Program Manager, and Assistant Director of Research in support of the clinical trials. Establishes liaisons with relevant parties at the Medical Center that may include: Collaborating and referring providers (physicians, nurses, etc..), Research Nurses, Research Pharmacists, Program Managers, Medical Technicians, Clinical Information Systems and regulatory Services. Might assist in the initiation and management of research studies.Job Responsibilities: * Human Subjects' Research - As applicable, prepares and completes the submission of necessary documents required by theNYUInstitutionalBoard(IRB),NYUOfficeofClinicalTrials, Bellevue Hospitals Research Committee,andanyotherappropriatepartiesinorderto obtain approval to conduct human subjects research (e.g., ensures the update and submission of necessary documents and/or forms to appropriate destination). Might prepare, audit and submit monthly enrollment statistics to the Office of Clinical Trials, and provides other information in timely manner, as necessary. * StudyRegulations-Awareofstudyregulatorystatusandkeepanuptodatecopyofregulatorydocuments. Conducts the informed consent process and ensure that the patient/subject fully understands what is requiredofthemthroughoutthestudy.Followsthroughregularlywiththepatient/subjectsremindingthemof visits and compliance. May monitor any outward effects or issues regarding patient/subject safety andreport this to the Principal Investigator, clinician, and manager. * Data Management - Responsible for collecting and auditing patient information for the research project(s). This may include abstraction of data from the patient chart (e.g., laboratory or diagnostic test results, surgical/radiationtreatmentsdelivered,adversedrugreactions,etc);abstractionofdataforpublications,or data collection from outside physicians offices. Audits and manages data from and into the database. Prepares forms and reports, compiles and analyses data, statistics, and other materials for reports. Conducts study visits, obtains and documents information within the time frame specified. * Budget Assists with development of a preliminary draft budget and submit to the PM/Asst. Director/Principal Investigator. Reviews sponsor-proposedbudgetforadequatecoverage of PI and coordinator time and effortandrecommendchangesasappropriate.Assistsinthe preparation of funding repor

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