---
title: 'Director of Clinical Affairs at Eight Sleep'
canonical: 'https://feeny.ai/job/director-of-clinical-affairs-eight-sleep-boston-j98qdj73hxz9'
type: 'job'
last_seen: '2026-10-20'
---

# Director of Clinical Affairs at Eight Sleep

- **Company:** Eight Sleep
- **Location:** Boston, MA
- **Employment:** full-time
- **Work type:** hybrid
- **Posted:** 2026-08-16
- **Last confirmed live:** 2026-10-20
- **Apply:** https://jobs.ashbyhq.com/eightsleep/3a7a9940-8137-4f9d-becd-e981de527218

## Job description

## JOIN THE SLEEP FITNESS MOVEMENT

At Eight Sleep, we're on a mission to fuel human potential through optimal sleep. As the world's first sleep fitness company, we're redefining what it means to be well-rested and building the most advanced hardware, software, and AI technology to make it possible. Our products power peak mental, physical, and emotional performance by transforming every night of sleep into a personalized, data-driven recovery experience. We are trusted by high performers, professional athletes, and health-conscious consumers in over 30 countries worldwide. Recognized as one of Fast Company's Most Innovative Companies in 2019, 2022, 2023, 2026, and twice named to TIME's "Best Inventions of the Year." We operate like a high-performance team: fast, focused, and motivated by impact. We don't just ship; we iterate, refine, and obsess over the details that help our members sleep better and wake up stronger.

High Standards. No Apologies. We operate with intensity because our mission demands it. At Eight Sleep, we bring the same mindset as the world's top performers: focused, relentless, and always pushing to be in the top 1% of our craft. Think Kobe Bryant's mamba mentality, applied to bold ideas, next-gen tech, and flawless execution. This isn't a 9-to-5. Our team is deeply committed, often putting in the extra effort — not because we're told to, but because we're invested. We're here to build fast, push limits, and deliver without compromise. If you thrive under pressure and want to do the most meaningful work of your career, you'll feel right at home. If you're looking for something easier — this isn't it.

## The Role

We're looking for a Director of Clinical Affairs who will own the end-to-end execution of our regulatory-driven clinical studies. This is a hands-on, operationally intense position for someone who knows how to stand up a study from scratch, manage third-party clinical sites, write IRB and informed consent documents, oversee data management, establish and oversee any study committees (EC, DSMB, etc.), prepare for FDA submissions and audits, and drive studies to completion on time and on budget. You'll be the connective tissue between our internal teams and the external clinical sites, investigators, IRBs, CROs, regulatory agencies, and, when necessary, study subjects directly. You'll bring deep fluency in regulatory requirements for medical devices, and you'll have a track record of delivering clinical studies that have supported regulatory submissions.

## What You'll Do

- Lead study design through collaboration with internal management, regulatory advisors, reimbursement specialists, and KOL advisory committees to ensure trials lead to successful clearance, payor coverage, and revenue ramp.
- Own clinical study execution from protocol development through final study report — including feasibility, site selection, activation, enrollment management, monitoring, and close-out.
- Write and manage IRB/Ethics submissions, informed consent forms (ICFs), and all study-related essential documents.
- Select, qualify, and oversee third-party clinical sites and investigators. Serve as the primary point of contact for site teams, ensuring protocol compliance, enrollment targets, and data quality.
- Manage clinical data operations, including CRF/eCRF design, data review, query resolution, and coordination with data management vendors or internal teams.
- Communicate directly with study sites and subjects as needed — you're comfortable picking up the phone and solving problems in real time.
- Develop and maintain study timelines, budgets, and risk mitigation plans. Flag issues early, propose solutions, and keep leadership informed with clear, concise reporting.
- Ensure compliance with FDA regulations (21 CFR Parts 11, 50, 56, 812, 820), ICH-GCP, ISO 14155, and applicable SaMD guidance documents.
- Manage relationships with CROs and other clinical vendors, including contract negotiation, performance oversight, and issue resolution.
- Collaborate cross-functionally with regulatory affairs, product, engineering, data science, and legal teams to ensure clinical strategies align with product development and submission timelines.
- Participate in regulatory interactions with the FDA and other notified bodies/ agencies by supporting your RA/QA peers in the creation of pre-subs, 510(k) submissions, and other correspondence.
- Build and scale the clinical operations function — develop SOPs, templates, tracking systems, and processes that can grow with the company.

## What You Bring

- 10+ years of hands-on clinical operations experience, with at least 5 years of experience in leadership roles, executing clinical studies for FDA-regulated medical devices, SaMD/digital health products, or combination products. We want someone who has designed, run, and successfully translated trials into regulatory approvals and marketed products.
- Track record of leadership or critical participation in trial(s) that led to new FDA clearances/approvals or meaningful labeling expansions for existing products.
- Demonstrated experience managing third-party clinical sites, including site selection, activation, monitoring, and close-out.
- Proven ability to author IRB/Ethics submissions, informed consent forms, and clinical protocols.
- 7+ years experience of cross-functional program management, involving clinical, engineering, and regulatory teams.
- Strong working knowledge of clinical data management — eCRF design, data cleaning, query management, and database lock processes.
- Fluency in FDA device regulations (IDE, De Novo, 510(k) clinical requirements), ICH-GCP, ISO 14155, and familiarity with SaMD-specific guidance (e.g., FDA Digital Health frameworks).
- Experience with clinical study budgeting, vendor management, and CRO oversight.
- Familiarity with the documentation and adjudication of AEs, device deficiencies, and associated reporting requirements.
- History of cultivating KOL relationships for participation in protocol development, research partnerships, study sub-committees, manuscripts/presentations/symposia, and related activities.
- Excellent written and verbal communication — you can draft a protocol, run a site initiation visit, and present enrollment updates to executives with equal confidence.
- Bachelor's degree required; advanced degree (MS, MPH, PhD, or clinical doctorate) preferred.
- ACRP or SOCRA certification is a plus.

Bonus Points

- Experience with biosensing devices, consumer health technology, or wellness platforms pursuing clinical validation.
- Familiarity with real-world evidence (RWE) study designs and decentralized / hybrid clinical trial models.
- Prior experience in a high-growth startup or scale-up environment where you had to build processes from the ground up.
- Experience supporting FDA breakthrough device designations or pre-submission meetings.

Why Join Eight Sleep? Innovation in a culture of excellence. Our flagship product, the Pod, is beloved by hundreds of thousands of customers worldwide. You will be part of a team that continuously pushes the boundaries of technology in sleep fitness. Immediate responsibility and accelerated career growth. From your first day, you'll take on substantial responsibilities that have a direct impact on our core business and product success. We are a small team that empowers you to own your projects and see the tangible effects of your efforts. Work alongside other bright minds like you. At Eight Sleep, exceptional intelligence and a passion for breakthroughs are the norms. Equity participation. We extend equity to every full-time team member, recognizing and rewarding your direct contributions to our success — including periodic equity refreshes based on performance. Your own Pod. Every Eight Sleep employee receives the very product that defines our mission. You'll also get full access to health, vision, and dental insurance for you and your dependents, plus other perks.

## Compensation

Target Base Salary: $200,000 – $250,000* *Compensation is based on experience, qualifications, and market benchmarks for the respective location you will be based in (i.e. SF or Boston). Equity and performance-based incentives are a significant component of total compensation at Eight Sleep.

At Eight Sleep we continually celebrate the diverse community different individuals cultivate. As an equal opportunity employer, we stay true to our values by ensuring everyone feels they can flourish and grow. We are committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, or Veteran status.

## About Eight Sleep

## Company Overview
- **One-liner**: Eight Sleep builds an AI-driven, always-on predictive health platform powered by sleep, using a smart bed cooling system to measure physiology, regulate temperature, and improve recovery and long-term health.
- **Entity Type**: Private (profitable as of 2025; latest raise: $50M at $1.5B valuation)
- **Headquarters**: New York, New York, USA (also offices in San Francisco, Boston, Milan)
- **Founded**: 2014
- **Founders**: Matteo Franceschetti (CEO), Massimo Andreasi Bassi (CTO), Alexandra Zatarain (CMO)

## Core Business
- **Primary industry**: Health-tech / Sleep fitness / Consumer wellness
- **Target customers**: B2C – consumers seeking better sleep, recovery, and long-term health (peri/post-menopausal women, athletes, biohackers)
- **Mission**: To fuel human potential through optimal sleep, building a predictive health system that turns the bed into an always-on health monitor.

## Products & Services
- **[Pod]**: Smart mattress cover (or topper) that uses thermoregulation, biometric sensing, and AI to cool, heat, and track sleep stages. Type: Hardware + SaaS + AI – subscription for advanced analytics and temperature profiles.
- **[Eight Sleep App]**: Companion mobile app that provides sleep scores, health insights (HRV, resting heart rate, respiratory rate), and personalized temperature schedules. Type: Software / Data platform.
- **[Predictive Health Platform]**: Upcoming AI-driven features that use longitudinal biometric data to predict health events (e.g., fever onset, illness, hormonal changes). Currently in research and development.

## Market Standing
- **Valuation**: $1.5 billion (post-$50M raise, March 2026)
- **Key Metric**: Over 200,000 active members nightly across 30+ countries; profitable since 2025
- **Notable Investors/Partners**: $150M+ total funding; lead investors include Y Combinator (S15 batch), Founders Fund? (Not fully listed, but $86M raise in 2021 at ~$500M valuation), recent $50M round at $1.5B in 2026.
- **Growth Signals**: 
  - Clinical studies show 32% improvement in sleep quality, 44% faster fall-asleep, 56% reduction in nighttime hot flashes for menopausal women
  - Expanded from NYC to SF, Boston, and Milan
  - 144 total employees, ~70 in product and tech

## Competitive Advantages
- **Integrated hardware/software/AI moat**: Patented thermal regulation combined with biometric sensors creates a data-flywheel that improves personalization over time.
- **First-mover in “sleep fitness”** – bridging consumer wellness and quantified health, with clinical validation (TIME Best Inventions, Fast Company Most Innovative).
- **Predictive health roadmap**: Moving beyond sleep tracking to proactive health alerts, a differentiator against generic wearables.

## Strategic Focus
- **Scale the predictive health platform**: Use the installed base of 200k+ sleepers to build an always-on diagnostic system; invest in AI and clinical research.
- **Expand internationally** (already in 30+ countries, focusing on EU and APAC).
- **Deepen B2B/clinical partnerships** – research collaborations for menopause, cardiovascular health, cognitive performance.

## Why Work Here
- **Culture** – “Bias for action”, ownership end-to-end, high impact (people in their 20s lead million-dollar projects). Emphasizes velocity and operational excellence (Kobe Bryant “mamba mentality” reference on careers page).
- **Work environment**: In-office for most hardware, ML, and R&D (SF), finance/brand/growth (NYC), clinical research (Boston). Some SWE and operations roles are hybrid or remote. Offices in 5 locations.
- **Perks**: Health insurance, dental, generous PTO, 401(k), equity, company-paid benefits, on-site workspaces in multiple cities.
- **Engineering culture**: Senior roles for embedded, backend, full-stack, clinical data. Compensation ranges e.g., Senior Backend $150K–$220K; remote options for specific roles (UK/Europe, US/CAN).

## Sources
1. [eightsleep.com/careers](https://www.eightsleep.com/careers/)
2. [builtin.com/company/eight-sleep](https://builtin.com/company/eight-sleep)
3. [ycombinator.com/companies/eight-sleep](https://www.ycombinator.com/companies/eight-sleep)
4. [eightsleep.com](https://www.eightsleep.com/)
5. [techcrunch.com (via YC page summary)](https://techcrunch.com/2021/08/19/eight-sleep-raises-86m/)

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