Clinical Research Coordinator I
Mount Sinai Health System
New York, NYFresher1h agovia LinkedIn
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 agency, and administering lifestyle questionnaires.
- Assists in preparing grant applications, IRB/GCO for submission 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 closely related field.
- One year of research experience preferred.
- No experience required.
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 e.g., Institutional Review Board, Grants and Contracts Office).