Clinical Research Coordinator: Data, Consent & Study Support

Mount Sinai; United States; On-site; USD 52,000 - 76,000; Full time

Job summary

Mount Sinai seeks an entry-level Clinical Research Coordinator to assist in clinical studies under the supervision of PI or senior staff. The role involves obtaining informed consent, recruiting and screening participants, and managing study data within Mount Sinai policies.

The coordinator will support grant applications and regulatory submissions, maintain accurate source documents, and may assist with specimen handling and site visit preparations.

Qualifications

• Bachelor's degree preferred for candidates.
• 0-2 years of research/human subjects experience preferred or required.

Responsibilities

• Conduct routine and standardized human subjects research under supervision.
• Obtain informed consent and screen participants for eligibility.
• Collect, maintain and organize study data.
• Assist in grant submissions and regulatory documentation (IRB, Grants and Contracts Office).
• Maintain source documents and confidential data.
• May secure and ship clinical specimens as required by the protocol.
• May assist in regulatory agency site visits.
• Perform other related duties.

Skills

Informed consent

Data collection

Participant interviewing

Regulatory basics

Education

Bachelor's degree in science or related field

Job description

Mount Sinai seeks an entry-level Clinical Research Coordinator to assist in clinical studies under the supervision of PI or senior staff. The role involves obtaining informed consent, recruiting and screening participants, and managing study data within Mount Sinai policies.

The coordinator will support grant applications and regulatory submissions, maintain accurate source documents, and may assist with specimen handling and site visit preparations.