Clinical Research Coordinator I — Entry‑Level Study & Data Coordination

Mount Sinai Health System; United States; On-site; USD 55,000 - 75,000; Full time

Job summary

Mount Sinai Health System seeks a Clinical Research Coordinator to support daily operations of clinical studies, including obtaining informed consent, collecting and organizing data, and ensuring accurate documentation. The role involves inputting data into databases, maintaining source documents, coordinating with IRB submissions, and assisting with grant applications.

A Bachelor's or Master's degree in science is required; no prior experience is necessary though 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 and inputs into database.
• Obtains informed consent and educates participants.
• Screens participants for eligibility and assists with visits and questionnaires.
• Assists in preparing grant applications, IRB/GCO submissions.
• Maintains source documents and subject files.
• Secures, delivers and ships clinical specimens as required by the protocol.
• Prepares for monitoring visits.
• Performs other related duties.

Skills

Informed consent

Data collection

Record keeping

Education

Bachelor's or Master's degree in Science

Job description

Mount Sinai Health System seeks a Clinical Research Coordinator to support daily operations of clinical studies, including obtaining informed consent, collecting and organizing data, and ensuring accurate documentation. The role involves inputting data into databases, maintaining source documents, coordinating with IRB submissions, and assisting with grant applications.

A Bachelor's or Master's degree in science is required; no prior experience is necessary though 1 year of research experience