Teams at Hawthorne Health, Inc.

Serve as the Principal Investigator providing clinical oversight for sponsor-initiated trials: manage site compliance with protocol, GCP, and regulations; supervise and train site staff; review assessments, labs and diagnostics; make medical decisions on enrollment and adverse events; ensure data accuracy and investigational product accountability; liaise with sponsors/CROs/IRBs; participate in visits, audits, and inspections; maintain medical education.

The Clinical Research Coordinator will manage clinical trial activities, including patient recruitment, data management, and adherence to regulatory requirements, with potential for full-time advancement.

The Clinical Research Coordinator will manage clinical trial activities, including patient recruitment, data entry, and compliance with regulations while ensuring site operations run smoothly.