Clinical Research Coord I — Pathology & Molecular

Mount Sinai

New York (NY)

On-site

USD 59,000 - 74,000

Full time

12 days ago

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Job summary

The Mount Sinai Health System in New York invites applications for a Clinical Research Coordinator who will assist in daily activities of clinical studies, obtain informed consent, collect and organize data, and prepare samples for analyses.

The role supports grant applications, IRB submissions, and regulatory filings. Strong attention to detail and clear communication are essential as you coordinate data and ensure compliance across study sites.

Qualifications

  • Bachelor's or Master's degree in science or closely related field.
  • No experience required; one year of research experience preferred.

Responsibilities

  • Collects and records study data. Inputs all information into database.
  • Obtains informed consent under minimal supervision and educates participants about study requirements.
  • Assists with clinical research activities including screening participants, registering subjects, and administering lifestyle questionnaires.
  • Assists in preparing grant applications, IRB/GCO submissions, and filings.
  • Maintains source documents and subject files and ensures complete compilation of data through chart reviews.
  • Secures, delivers and ships clinical specimens as required by the protocol.
  • Prepares for monitoring visits.
  • Performs related duties including sample preparation using immunological techniques and maintains data/results.

Skills

Communication skills
Attention to detail

Education

Bachelor's/Master's in Science

Job description

The Mount Sinai Health System in New York invites applications for a Clinical Research Coordinator who will assist in daily activities of clinical studies, obtain informed consent, collect and organize data, and prepare samples for analyses.

The role supports grant applications, IRB submissions, and regulatory filings. Strong attention to detail and clear communication are essential as you coordinate data and ensure compliance across study sites.

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