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New York Medical College

Clinical Research Coordinator

Clinical Research OperationsUpdated on Nov 14
Full-timeHawthorne, NY, USA$43.7k - $54.6k /yrIn-person

About the Job

Requirements

  • A bachelor's degree is required; a health-science field is preferred.
  • Proficiency with Microsoft Office, including Word, Excel, and Outlook.
  • Ability to track multiple projects and work independently.
  • Strong problem-solving, communication, and analytical skills.

Responsibilities

  • Review and analyze clinical trial protocols and informed consent forms.
  • Assist the Principal Investigator and Sub-Investigator with the study start-up process.
  • Coordinate budget reviews and Institutional Review Board reviews.
  • Submit regulatory documents and communicate with the Institutional Review Board.
  • Enter data and manage queries.
  • Manage supplies of investigational study drugs and monitor their temperature.
  • Invoice the study sponsor for study procedures according to contract requirements.
  • Coordinate transportation and lodging as needed, and submit patient travel and meal receipts to the sponsor.
  • Manage medical supplies and related product orders.
  • Pack and ship clinical laboratory specimens.
  • Maintain source documents in accordance with Food and Drug Administration and Good Clinical Practice guidelines.
  • Perform other assigned duties.

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