Noho Labs - Research Coordinator
About The Position
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.
Requirements
- Post-baccalaureate candidate, graduate student, or early-career clinical research professional
- Interested in clinical research
- Interested in longevity and performance medicine
- Interested in peptide therapeutics
- Interested in human subjects research
- Interested in digital health or telehealth-enabled care
- Interested in research operations at an early-stage company
Nice To Haves
- 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
Responsibilities
- 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
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
Education Level
No Education Listed
