About The Position

The Clinical Research Coordinator is an entry-level human subjects researcher who conducts and assists with clinical research studies under the supervision of the Principal Investigator or senior clinical research staff. The coordinator obtains informed consent and collects, maintains, and organizes study information. The role also assists with preparing and submitting grant applications and related documents, including Institutional Review Board and Grants and Contracts Office materials.

Requirements

  • 0–2 years of research or human subjects experience.
  • A bachelor's degree in science or a related field is preferred, or a combination of relevant research experience and education.

Nice To Haves

  • Bachelor's degree in science or a related field.

Responsibilities

  • Conduct routine and standardized human subjects research using appropriate research or interview techniques specific to the project, under direct supervision of the Principal Investigator or senior clinical research staff.
  • Assist with clinical research activities, including obtaining informed consent, screening participants for eligibility, registering patients with sponsoring agencies, administering questionnaires, and answering telephone calls.
  • Assist with collecting, analyzing, and reviewing experimental data for publication and presentation.
  • Maintain source documents and subject files in accordance with Mount Sinai policies and procedures, ensuring accurate, confidential, and complete data compilation.
  • Secure and ship clinical specimens as required by the protocol, when needed.
  • Assist in preparing for regulatory agency site visits, when needed.
  • Perform other related duties.
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