Clinical Research Coordinator: Study Operations & Data

Mount Sinai Morningside

New York (NY)

On-site

USD 58,661 - 73,530

Full time

14 days+

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Job summary

Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study data, and assist with grant applications. The role involves collaborating with investigators and research staff to ensure protocol compliance.

No prior experience is required, though one year of research experience is preferred; a science degree is required.

Qualifications

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

Responsibilities

  • Collects and records study data and inputs all information into a 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, IRB/GCO submissions, 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.

Skills

Data collection
Informed consent administration

Education

Bachelor's or Master's degree in science or related field

Job description

Mount Sinai Morningside is seeking a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study data, and assist with grant applications. The role involves collaborating with investigators and research staff to ensure protocol compliance.

No prior experience is required, though one year of research experience is preferred; a science degree is required.

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