Clinical Research Assistant I - ISM, Surgery

Mount Sinai Health System

United StatesFull time
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Location
United States
Job type
Full time
Posted
Oct 2
18 days ago
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About the company

Mount Sinai Health System

Hospital & health care · 10,001+ employees

Mount Sinai Health System on LinkedIn

What you'll do

  • Supports clinical research studies by screening and registering participants, collecting and entering study data, and maintaining study files.
  • Assists with grant and IRB submissions, monitoring visits, and specimen handling.

What you need

  • Associates Degree in Science or closely related field preferred or HS/GED plus two years of related experience
  • 1 year in research environment preferred
  • Education: an associate degree or a high school diploma

Key skills

Associates Degree in Sciencerelated experienceresearch environment

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Read the full posting here
The Clinical Research Assistant I assists in the daily activities of clinical research studies, including collection and organization of study information. Assists in preparing grant applications and documents (e.g., Institutional Review Board, Grants and Contracts Office), and provides clerical support to Clinical Research Coordinators and others in assigned area. Associates Degree in Science or closely related field preferred or HS/GED plus two years of related experience 1 year in research environment preferred Non-Bargaining Unit, 862 - Surgery - ISM, Icahn School of Medicine Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires. Collects and records study data. Inputs all information into database. Assists in preparing grant applications, IRB/GCO for submission and filings. Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through chart reviews. Secures, delivers and ships clinical specimens as required by the protocol. Assists in the preparation for monitoring visits. Performs other related duties.

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