Clinical Research Coordinator

Noho Labs

Remote regions

US

Benefits

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Study Startup and Regulatory Coordination:

  • Support IRB submission processes, including Advarra-related documentation and correspondence.
  • Conduct literature reviews to inform protocol development and draft informed consent forms and recruitment materials.

Study Operations and Recruitment:

  • Coordinate patient recruitment, screening, enrollment, and follow-up workflows across Noho's clinical infrastructure.
  • Track milestones and participant progress while maintaining accurate, organized research records.

Data, Reporting, and Dissemination:

  • Clean, organize, and manage study data for interim review and final analysis.
  • Prepare preliminary data summaries and support external presentations and manuscript development.

Noho Labs

Noho Labs operates at the intersection of performance, longevity, and personalized medicine by providing clinician-led education and safety-first therapies. It is an early-stage company building a modern longevity and performance platform through partnerships with a physician-led telehealth practice.

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