Clinical Research Coordinator I- Division of Pulmonary, Critical Care and Sleep Medicine
About The Position
The Division of Pulmonary, Critical Care and Sleep Medicine at the Icahn School of Medicine at Mount Sinai is seeking a Clinical Research Coordinator I. The division conducts multidisciplinary clinical and translational research with state-of-the art equipment and cutting-edge technology for diseases and disorders across the lifespan. 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). We are seeking a highly motivated and organized Clinical Research Coordinator (CRC) to join our research team. The CRC will play a crucial role in supporting the clinical research project by focusing on participant recruitment, scheduling, and conducting study visits. This position offers the opportunity to contribute to groundbreaking research while working closely with faculty investigators, research staff, and study participants.
Requirements
- Bachelors or Masters degree in Science or closely related field.
- No experience required.
- One year of research experience preferred.
Nice To Haves
- Bachelors or Masters degree in Science or closely related field.
- 1-2 years of research experience.
- Patient facing experience is preferred.
Responsibilities
- Collects and records study data.
- Inputs all information into 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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Number of Employees
5,001-10,000 employees
