Noho Labs - Research Coordinator

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.

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.

**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**

• 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

• 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

• 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

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

• 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