Clinical Research Coordinator I: Study Ops & IRB Support

A healthcare provider in New York is seeking a Clinical Research Coordinator to assist in daily research activities. Responsibilities include collecting and recording data, obtaining informed consent, and preparing grant applications. The ideal candidate will hold a Bachelor’s or Master’s degree in a relevant field and have 1-2 years of research experience. This role supports vital clinical studies and ensures compliance with hospital procedures. #J-18808-Ljbffr