Job Description

Introduction
To heal, to teach, to discover and to advance the health of the communities we serve.
To learn more about the “Montefiore Difference” – who we are at Montefiore and all that we have to offer our associates, please click here.
Overview
The Cancer Clinical Trials CRC I under direct supervision supports the research team in overall conduct of clinical trials using Good Clinical Practice. Mentored by an experienced Clinical Research Coordinator III the CRC I is responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials.
Responsibilities
Collects and records study data. Inputs all information into database.
Ensures timely collection of protocol related samples including shipment to outside entities as required.
Obtains informed consent for non-interventional studies.
Administers questionnaires.
Participates and supports investigators in the informed consent process for interventional trials.
Collects, maintains, and organizes study information including compilation, registration, and submission of data, as required by the Sponsor.
Attends clinic as needed to perform activities.
Requirements
Bachelor's Degree Required, Master's degree preferred.
ACRP (or SOCRA) certification preferred.
Ability to use MS Office.
Good organizing and prioritizing skills.

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