Clinical Research Coordinator I
Mount Sinai Morningside
New York, NYFresher46m agovia LinkedIn
About the Role
The Clinical Research Coordinator I - Rehabilitation and Human Performance assists in the daily activities of clinical research studies.
Key Responsibilities
- Collects and records study data, inputting all information into a database.
- Obtains informed consent under minimal supervision and educates participants regarding study requirements.
- Assists with clinical research study activities, including answering phone calls, screening participants for eligibility, registering subjects with sponsoring agencies, and administering lifestyle questionnaires.
- Assists in preparing grant applications and documents for the Institutional Review Board (IRB) and Grants and Contracts Office (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.
- No experience required.
- One year of research experience preferred.
Qualifications
No specific qualifications listed beyond educational background and experience preference.