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Clinical Trials Coordinator - Data & Compliance Focus

Job in Town of Mount Pleasant, Westchester County, New York, USA
Listing for: Touro University
Full Time position
Listed on 2026-10-14
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 43680 - 54600 USD Yearly USD 43680.00 54600.00 YEAR
Job Description & How to Apply Below
Location: Town of Mount Pleasant

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.

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)

Responsibilities

  • Review and analysis of clinical trial protocols and informed consent forms
  • Assist Principal and Sub-Investigator in study start-up process
  • Coordinate budget review and IRB reviews
  • Submission of regulatory documents and communication with IRB
  • Data entry, management of queries
  • Managing supply of investigational study drug with temperature monitoring
  • Invoicing Study Sponsor for study procedures as per contract requirements.
  • Coordinating transportation and lodging (as needed) with submission of patient travel and meal receipts to Sponsor
  • Management of medical supplies and related product orders
  • Packing and shipping of clinical laboratory specimens
  • Maintain source documents in accordance with FDA and GCP guidelines
  • Other duties as assigned
Qualifications

  • 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.
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