Research Associate

New York University School of Medicine

United States

June 10, 2022

Description

Job Responsibilities:

 Generates hypotheses and designs and performs experiments to test them.
 After a period of time working in the laboratory, the candidate will be expected to train graduate students and post-doctoral fellows in experimental design, technique and performance.
 Participates in the editing and proofing of grant proposals, annual grant reports, and manuscripts for publication and recommends modifications to the Principal Investigator.
 Contributes to the preparation of articles on research outcomes and progress and to the submission of same for publication.
 Reads and understands relevant scientific literature.
 Presents findings at lab meeting, responds to challenges, and participates in exchanges of ideas to advance the science.
 Demonstrates a significant level of intellectual input into the design of the project.
 Communicates results and collaborates with other professionals in the lab.
 Prepares figures and diagrams for presentations and publications.
 Based on results, independently suggests and tests modifications to protocols.
 Records all experimental findings in a laboratory notebook, analyze and interpret experimental findings.
 Executes multiple experiments simultaneously over time independently.

Additional Position Specific Responsibilities: Responsible for assisting with various research and evaluation tasks conducted at the Medical Center, including literature reviews, searches for funding opportunities, publication/presentation activities, and IRB/data management for existing studies. Ensures the accurate execution of protocols in accordance with Good Clinical Practices, HIPAA and required obligations to patient/subject, Principal Investigator, research team and the sponsor. Interfaces directly with patients/subjects and the Principal Investigator in support of applicable projects. Specific Responsibilities: NYU Health and Human Services Office of Clinical Trials/IRB. If applicable, assists in the submission of necessary documents required by the NYU Institutional Board (IRB), Office of Clinical Trials in order to obtain approval to conduct human subjects research. Secures accurate signatures and forwards documents and/or forms to appropriate destination. 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 the sponsor. Seek out funding opportunities and assisting in the assembly of grant applications. Reporting and Dissemination: Assists in the preparation of publications and presentations, including conducting literature reviews, formatting and preparing manuscripts for journal submissions. Study Regulations – Assists with the informed consent process and ensures that the patient/subject fully understands what is required of them throughout the study. Monitors any outward effects or issues regarding patient/subject safety and report this to the Principal Investigator, Physician and Research Nurse. Assists with the informed consent process and ensure that the patient/subject fully understands what is required of them throughout the study. Reminds patient/subjects of visits and compliance in a consistent manner.

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