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Associate Research Coordinator
Job in
New York City, Richmond County, New York, USA
Listed on 2026-02-06
Listing for:
NYU Langone Medical Center
Full Time
position Listed on 2026-02-06
Job specializations:
-
Healthcare
Clinical Research, Medical Science
Job Description & How to Apply Below
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 to med.nyu.edu, and interact with us on Linked In, Glassdoor, Indeed, Facebook, Twitter and Instagram.
Position Summary:
We have an exciting opportunity to join our team as an Associate Research Coordinator.
In this role, the successful candidate is responsible for providing moderate to advanced range of coordination of research studies conducted at NYU Langone Health Medical Centers assists with the recruitment enrollment grant submissions research data collection and study coordination activities. Serves as liaison with internal and external funding agencies. Ensures the accurate execution of research protocols in accordance with Good Clinical Practices HIPAA FDA and required obligations to research participants, Principal Investigators, the Research Team, and sponsors.
Interfaces directly with patients/subjects and Principal Investigators in support of the clinical trials if applicable.
Establishes liaisons with relevant parties at the Medical Centers that may include:
Research Nurses, Research Pharmacists, Program Managers, Medical Technicians, Clinical Information Systems, and Regulatory Services Might assist in the initiation and management of research studies. Works under general direction or the Project Manager and Principal Investigators.
Job Responsibilities:
* Human Subjects Research - As applicable oversee the submission of necessary documents required by the NYU Institutional Board IRB NYU Office of Clinical Trials and any other appropriate parties in order to 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;
* Study Regulations - Aware of study regulatory status and keep an up to date copy of regulatory documents;
Study Activities
* Assists with the informed consent process and ensure that the patient/subject fully understands what is required of them throughout the study
* Follows through regularly with the patient/subjects reminding them of visits and compliance;
* May monitor any outward effects or issues regarding patient/subject safety
Minimum Qualifications:
To qualify you must have a Bachelor's degree in life sciences, allied health or equivalent in a related discipline and 0-1 years experience or an equivalent combination of education and experience. Effective oral, written, communication, interpersonal skills. Must be able to work under the direction of supervision. Ability to operate research related equipment. Proficiency in using various Microsoft Office applications such as World, Excel, Access, Power Point and Outlook.
Familiar with Internet applications. Ability to identify, analyze and solve problems. Time management skills and ability to work well under pressure.
Preferred Qualifications:
Knowledge of basic medical terminology is preferred. Prior experience working with Research Protocols. Experience working in an academic medical center environment
Qualified candidates must be able to effectively communicate with all levels of the organization.
NYU Grossman School of Medicine provides its staff with far more than just a place to work. Rather, we are an institution you can be proud of, an institution where you'll feel good about devoting your time and your talents. At NYU Langone…
Position Requirements
10+ Years
work experience
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