New York Medical College·Town of Mount Pleasant, New York
The coordinator will manage clinical trial protocols, IRB submissions, and regulatory documentation for investigational drug studies. Responsibilities also include data management, supply monitoring, and the handling of clinical laboratory specimens.
Overview The Division of Medical Genetics at New York Medical College is seeking a clinical research coordinator to work with our team on multiple clinical trials. The ideal candidate has 2 years of clinical trial experience, but we are willing to train the right candidate. The coordinator will be working on investigational drug studies as well as prospective and retrospective data entry for multiple studies.
Category: Full-time, Grant Supported Position-(Position is contingent on continued funding)
Bachelor's degree required, preferably in health-science field Proficiency with Microsoft Office suite, including Word, Excel, and Outlook Must be adept at keeping track of multiple projects, able to work independently, and have strong problem solving, communication, and analytical skills Minimum Salary USD $43,680.00/Yr. Maximum Salary USD $54,600.00/Yr.
A bachelor's degree, preferably in a health-science field, and proficiency in Microsoft Office are required. The ideal candidate has 2 years of clinical trial experience and strong organizational and analytical skills.
Market context
Clinical research coordinator roles in New York are often tied to hospitals, academic medical centers, and research networks, so demand is typically strongest where active studies and regulatory oversight are concentrated. These positions are competitive because employers look for candidates who can manage protocols, documentation, EMR use, and compliance with GCP and CLIA; a STEM background and lab experience can help, and a bachelor’s degree is often preferred. Review the AI-summarized requirements and benefits here to save time, then tailor your application to show research coordination, regulatory, and EMR experience.
