8VC - Noho Labs

• 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