[Hiring] Clinical Research Coordinator @8VC

Role Description

Noho Labs is seeking a Clinical Research Coordinator to help launch and operate human clinical research studies focused on peptides, safety, tolerability, and early signals of efficacy in real-world care settings. This role is ideal for someone who wants meaningful ownership at an early-stage company and is excited by the opportunity to help build the research engine behind a modern longevity and performance platform. The coordinator will work across study startup, patient recruitment, data collection, regulatory coordination, and dissemination of findings. This is not a passive support role. It is a highly hands-on position for someone who is organized, analytical, comfortable with ambiguity, and motivated by the chance to help shape how high-quality clinical evidence is generated in an emerging category.

What You’ll Do

• Study startup and regulatory coordination
  • Support IRB submission processes, including Advarra-related documentation and correspondence
  • Conduct literature reviews to inform protocol development and study materials
  • Draft informed consent forms, recruitment materials, case report forms, and other regulatory documents
  • Help organize investigator, site, and study files to support compliant research operations
  • Build and QA study questionnaires, intake flows, and research data collection tools
• Study operations and recruitment
  • Coordinate patient recruitment, screening, enrollment, and follow-up workflows
  • Help operationalize study launch across Noho’s clinical and research infrastructure
  • Track milestones, deadlines, and participant progress across active studies
  • Maintain accurate, organized, high-integrity research records and datasets
  • Partner with internal stakeholders to improve research workflows, dashboards, and reporting
• Data, reporting, and dissemination
  • Clean, organize, and manage study data for interim review and final analysis
  • Prepare preliminary data summaries and internal presentations
  • Support external presentations, abstracts, posters, and manuscript development
  • Work with statistical and clinical partners to help translate findings into credible, decision-useful outputs

What Success Looks Like

• Studies launch on time with strong operational structure and clean documentation
• Recruitment and follow-up processes run smoothly
• Research data is accurate, well organized, and usable for analysis
• Internal teams have visibility into study progress and outcomes
• Noho builds a stronger evidence base around peptide use, patient safety, and clinical outcomes

Qualifications

• Prior experience in clinical research, human subjects research, or healthcare research coordination
• Familiarity with IRB processes, informed consent, and research documentation
• Strong writing skills, especially for study materials, summaries, and presentations
• Comfort working with data collection tools, spreadsheets, and structured datasets
• Strong attention to detail and ability to manage multiple workstreams at once
• Interest in peptides, personalized medicine, chronic illness, recovery, or novel therapeutics
• Experience with remote research operations, patient-facing coordination, or startup environments is a plus