Clinical Research Coordinator I - Windreich Department of AI & Human Health
Mount Sinai Health System
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- Location
- United States
- Job type
- Full time
- Posted
- Oct 20
- 1 day ago
Career path
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About the company
Mount Sinai Health System
Hospital & health care · 10,001+ employees
What you'll do
- Collect, record, and enter study data into research databases
- Obtain informed consent and educate participants regarding study requirements and procedures
- Screen, recruit, and enroll subjects; schedule study visits and communicate with participants and clinical staff
- Support regulatory submissions and maintain study documentation
- Manage source documents and subject files; review medical records and compile subject data
- Operate and manage study-related technology and equipment
- Prepare and organize study records for monitoring visits
- Coordinate research procedures as required by the protocol
What you need
- Bachelors or Masters degree in Science or closely related field.
- No experience required. One year of research experience preferred.
- Education: a bachelor's degree or a postgraduate degree
Key skills
Informed consentData collectionResearch databasesRegulatory submissionsIRB applicationsStudy documentationSource documentsStudy technologyData verificationQuality control
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Read the full posting here
The Clinical Research Coordinator (CRC) will support the implementation and daily operations of the NeoNOVA study, a clinical research study evaluating AI-enabled video monitoring technology in neonatal care. The CRC will coordinate participant recruitment and enrollment, regulatory activities, study technology and equipment management, data collection, study documentation, and collaboration with clinical, research, and technical teams.
This position is ideal for candidates interested in clinical research, digital health, artificial intelligence applications in healthcare, and research operations. The CRC will gain experience working at the intersection of clinical research, technology, and neonatal care.
Bachelors or Masters degree in Science or closely related field.
No experience required. One year of research experience preferred.
Collects, records, and enters study data into research databases and supports data verification and quality control activities.
Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements and procedures.
Coordinates clinical research activities, including screening participants for eligibility, recruiting and enrolling subjects, scheduling study visits, maintaining study logs, and communicating with participants and clinical staff.
Supports the preparation and maintenance of regulatory submissions and study documentation, including IRB applications, amendments, continuing reviews, and sponsor-required materials.
Manages source documents and subject files in accordance with hospital procedures; reviews medical records and compiles subject data; and tracks screening, enrollment, and required study documentation to ensure timely completion.
Operates and manages study-related technology and equipment and coordinates research procedures as required by the protocol.
Prepares and organizes study records and documentation for monitoring visits.
Performs other related duties as assigned.