Clinical Research Coordinator I, Psychiatry
Mount Sinai Health System
New York, NYFresher48m agovia LinkedIn
About the Role
The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains, and organizes study information. Assists in preparing grant applications and documents for submission to the Institutional Review Board (IRB) and Grants and Contracts Office (GCO).
Key Responsibilities
- Collects and records study data, inputting all information into a database.
- Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
- Assists in activities related to clinical research studies, including answering phone calls, screening participants for eligibility, registering subjects with sponsoring agencies, and administering lifestyle questionnaires.
- Assists in preparing grant applications and IRB/GCO submissions and filings.
- Maintains source documents and subject files in accordance with hospital procedures.
- Ensures accurate and complete compilation of subject data through chart reviews.
- Secures, delivers, and ships clinical specimens as required by the protocol.
- Prepares for monitoring visits.
- Performs other related duties.
Requirements & Tech Stack
- Bachelors or Masters degree in Science or a closely related field.
- One year of research experience preferred.
Qualifications
- No experience required.