8VC

• Own the Noho Labs narrative • Build and refine Noho’s core messaging • Translate topics like peptides, longevity, hormone health, recovery, compounding, telehealth, and clinical care into language people understand and trust • Create messaging foundations including positioning, boilerplate, founder narrative, FAQs, patient education, launch messaging, and internal talking points • Write across formats: website copy, blog posts, patient education, email, social, press materials, founder posts, creator briefs, launch copy, and recruiting content • Build and execute Noho’s media strategy across health, wellness, business, technology, pharma, longevity, and lifestyle media • Identify and build relationships with the right journalists, podcasts, newsletters, creators, and industry voices • Write pitches, manage inbound and outbound media opportunities, prepare executives for interviews, and create briefing materials • Support launches, partnerships, research updates, clinical milestones, funding announcements, and sensitive communications • Shape the voice of Noho’s founder and leadership team across LinkedIn, X, podcasts, interviews, essays, panels, and speaking opportunities • Turn leadership ideas into sharp, high-signal content that builds credibility • Identify timely topics where Noho should have a point of view across peptide medicine, patient safety, telehealth, compounding, longevity, and personalized care • Own Noho’s social presence across relevant channels • Develop content that educates, builds trust, and makes Noho feel like a category-defining brand • Monitor trends across longevity, peptides, wellness, fitness, hormone health, GLP-1s, health tech, and patient communities • Identify timely opportunities to join the conversation and know when not to • Build Noho’s influencer and creator strategy across health, fitness, longevity, wellness, medicine, and lifestyle • Identify credible creators, practitioners, educators, podcasters, and community voices who can shape patient understanding • Manage outreach, briefs, approvals, content quality, and performance tracking • Create partnerships that feel authentic, educational, and brand-aligned • Create repeatable processes for content planning, media tracking, influencer outreach, social publishing, executive communications, and reporting • Build the communications calendar and ensure company moments are planned and executed well • Bring structure without slowing the company down

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

• Own the iOS member app end-to-end • Define mobile architecture and best practices • Build delightful UX for complex healthcare workflows • Integrate with our NestJS backend and Canvas Medical EHR • Implement push notifications, HealthKit integration, and offline-first patterns • Collaborate with product and design on new features • Potentially grow into managing mobile engineers as we scale