Clinical Research Coordinator I: Study Data & Consent

Mount Sinai; United States; On-site; USD 52,000 - 75,000; Full time

Job summary

Mount Sinai seeks a Clinical Research Coordinator to assist in daily management of clinical studies, obtain informed consent, collect and organize data, and support grant-related documentation.

The role involves data entry, participant screening, subject registration, and maintaining regulatory documents; supports monitoring visits and handling specimens. Requires a Bachelor's or Master's in science; no experience required, 1 year preferred.

Qualifications

• No experience required; one year of research experience preferred.
• Obtains informed consent under minimal supervision and educates participants regarding study requirements.
• Collects and records study data; inputs all information into database.
• Assists in preparing grant applications and documents (IRB, Grants and Contracts Office).
• Maintains source documents and subject files per hospital procedures; ensures data accuracy.
• Secures, delivers and ships clinical specimens as required by the protocol.
• Prepares for monitoring visits and performs other related duties.

Responsibilities

• Assist in daily activities of clinical research studies and obtain consent.
• Collect, record, and input study data into the database.
• Screen participants for eligibility and register subjects with sponsoring agency.
• Prepare grant documents and IRB/Grants and Contracts submissions.
• Maintain source documents and subject files per hospital procedures.
• Secure and ship clinical specimens and prepare for monitoring visits.
• Answer phone calls and perform other related duties.

Education

Bachelor's or Master's degree in Science or closely related field

Job description

Mount Sinai seeks a Clinical Research Coordinator to assist in daily management of clinical studies, obtain informed consent, collect and organize data, and support grant-related documentation.

The role involves data entry, participant screening, subject registration, and maintaining regulatory documents; supports monitoring visits and handling specimens. Requires a Bachelor's or Master's in science; no experience required, 1 year preferred.