Clinical Research Coordinator I
Mount Sinai Morningside
New York, NYFresher1h agovia LinkedIn
This job at a glance
- Who can apply
- New grads, no experience needed · Bachelor's degree or Master's degree
- Nice to have
- Patient care
- Work
- On-site in New York
- Pay
- Not stated by the employer.
- Skill demand
- Patient care85%of 99 similar entry-level jobs posted in the US this week
- Listed
- Nov 3, 2026 · still open
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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).
Key Responsibilities
- Collects and records study data. Inputs all information into a database.
- Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
- Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, 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.
- Cancer clinical trial experience preferred.
Qualifications
- No experience required.
- One year of research experience preferred.