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