Noho Labs - Research Coordinator
Clinical Research Coordinator
Noho Labs
Remote | Full-time
About Noho Labs
Noho Labs is building at the intersection of performance, longevity, and personalized medicine. Through clinician-led education and a safety-first approach, Noho helps patients explore evidence-based therapies, including peptides, with more rigor, better oversight, and higher quality standards than much of the broader market. Noho Labs partners with a physician-led telehealth practice focused on whole-body optimization, longevity, and wellness.
About the Role
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
Who This Role Is For
This role is well suited for a post-baccalaureate candidate, graduate student, or early-career clinical research professional interested in:
clinical research
longevity and performance medicine
peptide therapeutics
human subjects research
digital health or telehealth-enabled care
research operations at an early-stage company
Preferred Background
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