Clinical Research Coordinator: Data, Consent & Grants

Mount Sinai; New York (NY); Hybrid; USD 59.000 - 74.000; Vollzeit

Zusammenfassung

The Mount Sinai Health System in New York, NY is seeking a Clinical Research Coordinator to support daily study activities, obtain informed consent, and manage study data. You will assist in grant preparation, IRB submissions, and ensure compliance with hospital procedures. No prior experience required; research exposure is preferred.

Bachelor's or Master's in Science is required, with opportunities to grow in a leading academic medical system renowned for research and patient care.

Qualifikationen

• Bachelors or Masters in Science or closely related field.
• No experience required; one year of research experience preferred.

Aufgaben

• Collects and records study data; inputs into database.
• Obtains informed consent under supervision and educates participants.
• Assists with screening, subject registration, and lifestyle questionnaires.
• Supports grant applications, IRB/GCO submissions and filings.
• Maintains source documents and subject files per procedures.
• Secures, delivers, and ships clinical specimens as required.
• Prepares for monitoring visits; performs related duties.

Kenntnisse

Data collection

Informed consent

Data management

Communication

Ausbildung

Bachelor's or Master's degree in Science

Jobbeschreibung

The Mount Sinai Health System in New York, NY is seeking a Clinical Research Coordinator to support daily study activities, obtain informed consent, and manage study data. You will assist in grant preparation, IRB submissions, and ensure compliance with hospital procedures. No prior experience required; research exposure is preferred.

Bachelor's or Master's in Science is required, with opportunities to grow in a leading academic medical system renowned for research and patient care.