Clinical Research Coordinator I

About the Role

The Clinical Research Coordinator (CRC) will support the implementation and daily operations of the NeoNOVA study, evaluating AI-enabled video monitoring technology in neonatal care. 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.

Key Responsibilities

• Collects, records, and enters study data into research databases; supports data verification and quality control.
• Obtains informed consent under minimal supervision; educates participants regarding study requirements and procedures.
• Coordinates clinical research activities:
• Screening participants for eligibility.
• Recruiting and enrolling subjects.
• Scheduling study visits.
• Maintaining study logs.
• 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.
• Tracks screening, enrollment, and required study documentation to ensure timely completion.
• Operates and manages study-related technology and equipment.
• Coordinates research procedures as required by the protocol.
• Prepares and organizes study records and documentation for monitoring visits.
• Performs other related duties as assigned.

Requirements & Tech Stack

• Bachelors or Masters degree in Science or closely related field.
• No experience required.
• One year of research experience preferred.

Note: The provided text does not explicitly list a tech stack beyond general study technology and equipment.