Part-Time Clinical Research Coordinator | Data & IRB Prep

Mount Sinai Medical Center

New York (NY)

On-site

USD 23,419 - 52,348

Part time

14 days+

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Job summary

The Mount Sinai Health System is seeking a Part-time Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and manage data collection and documentation in accordance with hospital procedures.

This hourly position may involve overtime and requires completing tasks such as grant-related documentation, IRB submissions, and coordinating specimen shipments as per protocol.

Qualifications

  • Bachelor's degree in science or related field preferred or combination of relevant research experience and education.

Responsibilities

  • Collects and records study data and inputs all information into the database.
  • Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
  • Assists in activities related to clinical research studies, including answering phone calls, screening participants for eligibility, registering subjects with the sponsoring agency, and administering lifestyle questionnaires.
  • Assists in preparing grant applications and IRB/GCO for submission and filings.
  • Maintains source documents and subject files in accordance with hospital procedures and 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.

Education

Bachelor's degree in science or related field

Job description

The Mount Sinai Health System is seeking a Part-time Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, and manage data collection and documentation in accordance with hospital procedures.

This hourly position may involve overtime and requires completing tasks such as grant-related documentation, IRB submissions, and coordinating specimen shipments as per protocol.

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