Research Data Associate

Position Summary Join our team as a Research Data Associate. In this role you will provide direct data and/or clinical research support for clinical trials, studies, and general research under direct supervision. You will collaborate with school staff and departments, including Directors, Managers, Clinical Information Systems, Research Nursing, and Regulatory Services, and may interface with patients and their families. Job Responsibilities Interact with patients/subjects and families in a courteous and professional manner. Collaborate with various personnel involved in assisting with specific aspects of the study. Gather, properly package, store, and transfer slides, samples, and other important materials; coordinate shipment and transfer of varied types of materials among departments and labs. May complete assessments on study subjects/patients per protocol (with proper training); continue follow‑through with items and patients as part of the research study. May draw patients/subjects blood, perform EKG, and/or take vital signs if properly trained; may be required to travel to study initiation sites. Ensure protocol compliance by following standard steps regarding eligibility criteria, follow‑up process, and documentation. Demonstrate knowledge of policies and procedures of the host institution and regulatory requirements such as IRB and other approvals. Act as an internal auditor during quarterly internal audits for other studies; keep an up‑to‑date copy of regulatory documents. Initiate and continue regular contact with patients; encourage visit reminders and compliance to research while ensuring courteous, effective, professional interaction. Collect patient information using established methodologies; gather and compile data, statistics, and other materials as needed. Input clinical and non‑clinical data into databases or case report forms; extract data for publications or provide data collection from external physician offices; perform library searches and retrieve reference materials from various sources; request articles from medical journals. Compile data and assist in consolidating data for presentation to sponsors and regulatory agencies; review data with supervisor and provide reports to all parties (e.g., data and safety monitoring committee, principal investigator, sponsoring agency) on study progress. Recruit and screen potential patients/subjects for eligibility to the study. Minimum Qualifications Associate’s degree plus one year of related experience or an equivalent combination of education and experience. Computer literate with good interpersonal, writing, and verbal communication skills. Preferred Qualifications Bachelor's degree, preferably in science, public health, health education, or a related field. Prior experience in health care settings and/or research level interviews. Prior patient education experience. Benefits Our comprehensive benefits and wellness package includes financial security benefits, a generous time‑off program, and employee resource groups for peer support. All employees have access to our holistic employee wellness program, which focuses on physical, mental, nutritional, sleep, social, financial, and preventive care. The benefits and wellness package is designed to allow you to focus on what truly matters. Salary Range The salary range for the role is $29.56 - $29.56 Hourly. Actual salaries depend on a variety of factors, including experience, specialty, education, and hospital need. The salary range listed does not include bonuses, incentives, differential pay, or other forms of compensation or benefits. Equal Opportunity Employer NYU Grossman School of Medicine is an equal‑opportunity employer and is committed to inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration. Salary Transparency Notice To view the Pay Transparency Notice. #J-18808-Ljbffr NYU Grossman School of Medicine