Clinical Research Coordinator I
Mount Sinai Health System
New York, NYFresher1h agovia LinkedIn
About the Role
The Clinical Research Coordinator assists in the daily activities of clinical research studies. This role involves obtaining informed consent, collecting, maintaining, and organizing study information, and assisting in the preparation of grant applications and documents for 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 and educates participants on study requirements.
- Assists with clinical research study activities, including answering phone calls, screening participants for eligibility, registering subjects with the sponsoring agency, 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.
- Database knowledge.
- Familiarity with IRB/GCO procedures.
Qualifications
- No experience required.
- One year of research experience preferred.