Jobs at Hawthorne Health, Inc.

The Sub Investigator assists the Principal Investigator in managing clinical trials, ensuring protocol adherence, and overseeing patient safety while performing assessments and documenting study data.

Assist the Principal Investigator in managing clinical trials, ensuring adherence to protocols, providing medical oversight, and documenting study data accurately.

The Principal Investigator will oversee clinical trials, ensure adherence to protocols, manage research teams, and conduct patient assessments while maintaining ethical standards.

The Principal Investigator will lead clinical trials, manage site operations, oversee staff, ensure compliance, and maintain communication with stakeholders, focusing on participant care and data integrity.

The Principal Investigator leads clinical trials at a new research site, overseeing team management, ensuring protocol compliance, and making key medical decisions. Responsibilities include documentation, patient assessment reviews, and communication with sponsors.

The Principal Investigator will oversee clinical trials, ensuring compliance with guidelines, managing research staff, and making critical medical decisions regarding patient care and study protocols.

The Sub Investigator assists the Principal Investigator in managing clinical trials, ensuring protocol adherence, participant safety, and accurate data collection.

The Sub Investigator supports clinical trials by overseeing protocols, ensuring participant safety, performing assessments, and maintaining study compliance and documentation under the Principal Investigator's supervision.

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.

Provide PI oversight for clinical trials at the Fremont site: ensure GCP/ICH compliance, supervise site staff, review assessments and diagnostics, manage investigational product, communicate with sponsors/CROs/IRBs, participate in visits/audits, and ensure patient safety and accurate study documentation.

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.