Clinical Research Coordinator I - Windreich Department of AI & Human Health

HealthcareClinical Researcher
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Quick Summary

Overview

The Clinical Research Coordinator (CRC) will support the implementation and daily operations of the NeoNOVA study,

Technical Tools
HealthcareClinical Researcher

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.

  • 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.

 

 

 

 

 

 

 

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

 

 

Location & Eligibility

Where is the job
United States
On-site within the country
Who can apply
US

About this job

Who can apply
United States
Posted
Today
Employer
has 2,672 open jobs on Jobera.

Listing Details

Posted
October 20, 2026
First seen
October 20, 2026
Last seen
October 20, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
56%
Scored at
October 20, 2026

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Clinical Research Coordinator I - Windreich Department of AI & Human Health