(Clinical) Research 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 Associate. This role involves clinical research data collection, interaction with human subjects, and the maintenance of clinical research date data this role doesnot include bench science research.This is a per diem position with variable hours based on study needs, operational priorities, and candidates availability, offering scheduling flexibility; the role requires availability for early morning shifts (as early as 4:00 a.m.) and evening shifts (after 6:00 p.m.), as determined in coordination with the research team.Work collaboratively with a team of full-time Research Associates, Project Manager, and other study staff to contribute to shared study operations.Performs study procedures primarily in dialysis centers across all five boroughs of New York City, with occasional work in inpatient, outpatient, or other clinical settings.Conducts in-person and remote (over the phone, email, or text) patientrecruitment, data collection, and follow-up visits of participants who are enrolled in clinical trials and cohort studies.Conducts chart abstractions to ascertain clinical data.Administers behavioral, exercise and other interventions.Reports enrollment, follow-up, and retention rates for clinical trials and cohort studies.Prepares and maintains Standard Operating Procedures (SOPs) for clinicaltrials and cohort studies.Performs specimen processing and storage.Maintains study databases by entering, cleaning, and verifying data for accuracy and completeness.Coordinates communication between study sites, clinical staff, and research team members to ensure protocol adherence and timely data collection.Participates in study team meetings and contributes to protocol development, recruitment strategies, regulatory submissions, and process improvement discussions.Assists in the development and pilot testing of study instruments, surveys, and data collection tools.Prepares study materials such as recruitment flyers, participant packets, and consent forms.Schedules and documents study visits, maintaining detailed logs for tracking participant flow and study progress.Assists in the preparation of reports, abstracts, posters, and manuscripts for presentations and publications.Ensures compliance with Good Clinical Practice (GCP) and institutional policies related to participant safety, confidentiality, and data management.Monitors study supplies and coordinates with laboratory and clinical teamsto ensure proper inventory and equipment maintenance.Assists with quality assurance activities, including source document verification and internal audits.Supports grant and budget tracking, including study reimbursements and invoicing for multicenter projects.After a period of time working with the research team, the candidate will be expected to train newly hired Research Associates, graduate students, andpostdoctoral fellows in the study design, data collection, blood processing technique, and other aspects of the research.Job Responsibilities: * After a period of time working in the laboratory, the candidate will be expected to