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 Apply To This Job