Clinical Research Coordinator I: Study Data & Consent

Mount Sinai Medical Center

New York, Northern (NY, KY)

Hybrid

USD 59,000 - 74,000

Full time

4 days ago

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Job summary

Mount Sinai Health System in New York, NY seeks a Clinical Research Coordinator to support daily activities of clinical studies, obtain informed consent, collect and organize study data, and assist in grant applications and IRB submissions. The role involves maintaining source documents, shipping specimens as required, and preparing for monitoring visits.

Qualifications include a Bachelor's or Master's in Science; no experience required with a preference for 1 year of research experience.

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 of the investigator(s) and educates participants regarding study requirements.
Assists in screening participants for eligibility and registering subjects with sponsoring agency; administers lifestyle questionnaires.
Assists in preparing grant applications, IRB/GCO for submission and filings.
Maintains source documents and subject files; ensures complete compilation of data through chart reviews.
Secures, delivers and ships clinical specimens as required by the protocol; prepares for monitoring visits.