Clinical Research Coordinator — Research Data & Consent

Mount Sinai; Town of Madison (NY); On-site; USD 23,000 - 57,000; Full time

Job summary

Mount Sinai Health System in New York seeks a Clinical Research Coordinator to conduct and assist in clinical studies under supervision. You will obtain informed consent, collect and organize study data, and support grant submissions and regulatory documentation as needed.

The role involves coordinating with the Principal Investigator and senior staff, handling confidential data, and potentially assisting with regulatory visits and specimen handling.

Qualifications

• Bachelor's degree in science or related field required or equivalent experience.
• 0-2 years of research/human subjects experience preferred or required.

Responsibilities

• Conducts routine and standardized human subjects research under direct supervision.
• Assist in consent, eligibility screening, patient registration, questionnaires, and calls.
• Assist in collection, analysis and review of data for publication/presentation.
• Maintain source documents and subject files per Mount Sinai policies.
• May secure and ship clinical specimens as required by the protocol.
• Assist in preparation for regulatory agency site visits.
• Performs other related duties.

Education

Bachelor's degree in science or related field

0-2 years of research/human subjects experience

Job description

Mount Sinai Health System in New York seeks a Clinical Research Coordinator to conduct and assist in clinical studies under supervision. You will obtain informed consent, collect and organize study data, and support grant submissions and regulatory documentation as needed.

The role involves coordinating with the Principal Investigator and senior staff, handling confidential data, and potentially assisting with regulatory visits and specimen handling.