Jobs at Hawthorne Health, Inc.

Manage and support multiple clinical research sites across a multi-state territory. Provide operational leadership, ensure GCP/FDA/ICH/HIPAA compliance, support study startup and audit readiness, monitor performance metrics, build site relationships, coordinate sponsors/CROs/vendors, implement process improvements, and travel regularly to drive enrollment and operational excellence across the site network.

Serve as the onsite Principal Investigator overseeing clinical trials: ensure GCP/ICH/FDA compliance, supervise study staff, review assessments and diagnostics, make medical decisions, manage investigational product accountability, liaise with sponsors/CROs/IRBs, support audits/monitoring, and maintain clinical education.

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 Nurse Practitioner or Physician Assistant will assist the Principal Investigator in managing clinical trials, oversee participant safety, and maintain protocol adherence.

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.

Lead and oversee dermatology sponsor-initiated clinical trials as a part-time PI (1099). Ensure protocol compliance, GCP/ICH and FDA adherence, supervise site staff, review assessments and diagnostics, manage investigational product accountability, communicate with sponsors/CROs/IRBs, participate in visits and audits, and provide medical decision-making and oversight both on-site and remotely.

The Principal Investigator leads respiratory clinical trials, managing all trial aspects, overseeing a research team, ensuring protocol adherence, and making key medical decisions.