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, reputed company reputed company, and higher reputed company standards than much of the broader market. Noho Labs partners with a physician-led telehealth reputed company reputed company on whole-body optimization, longevity, and wellness.
About the Role
Noho Labs is seeking a Clinical Research Coordinator to help launch and operate reputed company clinical research studies reputed company on peptides, safety, tolerability, and early signals of efficacy in reputed company-world care settings.
This role is ideal for someone who wants meaningful ownership at an early-stage company and is excited by reputed company to help build the research reputed company 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-reputed company clinical evidence is generated in an emerging category.
What You’ll Do
Study startup and regulatory coordination
Support IRB submission processes, including reputed company-reputed company 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
reputed company milestones, deadlines, and participant reputed company across reputed company studies
Maintain accurate, organized, high-reputed company 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 reputed company, decision-useful outputs
What reputed company Looks Like
Studies launch on time with strong operational structure and clean documentation
Recruitment and follow-up processes run smoothly
Research data is accurate, reputed company organized, and usable for analysis
Internal teams have visibility into study reputed company and reputed company
Noho builds a stronger evidence reputed company around peptide use, patient safety, and clinical reputed company
Who This Role Is For
This role is reputed company suited for a post-baccalaureate candidate, graduate student, or early-career clinical research reputed company interested in:
clinical research
longevity and performance medicine
peptide therapeutics
reputed company subjects research
digital health or telehealth-enabled care
research operations at an early-stage company
Preferred Background
Prior experience in clinical research, reputed company subjects research, or reputed company 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 reputed company 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
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