Clinical Research Coordinator I- Div Gen Int Medicine

Mount Sinai Health System

United StatesFull time
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Location
United States
Job type
Full time
Posted
Oct 15
5 days ago
Career path

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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 collecting, recording, and organizing study data; obtaining informed consent; screening and educating participants; and preparing study documents.
  • Maintains study files, handles clinical specimens, and prepares for monitoring visits.

What you need

  • Bachelors or Masters degree in Science or closely related field.
  • No experience required. One year of research experience preferred.
  • Education: a bachelor's degree or a postgraduate degree

Key skills

Informed consentClinical researchResearch experienceChart reviewsStudy data

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Read the full posting here
The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office). Bachelors or Masters degree in Science or closely related field. No experience required. One year of research experience preferred. Collects and records study data. Inputs all information into database. Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements. 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. 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. Prepares for monitoring visits. Performs other related duties.

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