O

Owlet

Wearable infant health monitor and sleep

Medical Affairs

Physicians & SurgeonsConfirmed live in the last 24 hours
Full-timeRemote in USA

About the Job

Requirements

  • The candidate must have an MD or DO degree.
  • Board certification in Pediatrics is strongly preferred; other primary care or relevant clinical specialties, including family medicine, neonatology, and pulmonology, will be considered.
  • The candidate must have active or inactive medical licensure in the United States; active clinical practice is not required.
  • The candidate must have 3–7 years of combined clinical practice and/or industry experience in medical affairs, clinical development, or a medical science liaison role within medical device, digital health, consumer health, or life sciences.
  • The candidate must have direct patient care experience.
  • The candidate must be able to engage confidently with physicians, nurses, and other healthcare professionals as a peer.
  • The candidate must be able to translate clinical and scientific complexity into clear, accurate language for non-clinical audiences, including Sales, Marketing, and consumers.
  • The candidate must be comfortable operating across a broad scope in a lean, resource-constrained environment.

Responsibilities

  • Serve as Owlet's primary internal medical resource and clinical decision-making authority, advising across product development, safety, regulatory strategy, marketing, and long-term clinical and product strategy in collaboration with senior leadership.
  • Review and interpret adverse event reports, product complaints, and post-market safety signals; provide medical assessment, causality determination, and clinical recommendations to Quality, Regulatory, and Clinical Operations teams.
  • Support development of medical safety narratives for regulatory submissions, periodic safety update reports, and post-market surveillance activities; contribute clinical expertise to risk-benefit analyses and failure mode assessments.
  • Provide medical review and sign-off on clinical study protocols, informed consent forms, and clinical investigation plans prepared by Clinical Operations; support identification of external principal investigators where internal PI designation is not appropriate.
  • Advise Owlet's telehealth implementation and digital health initiatives by contributing clinical perspective to parent-facing care experiences, data labeling, feature development, and physician integrations intended to improve infant safety, health, and sleep.
  • Serve as Principal Investigator on Owlet-sponsored clinical investigations, including non-significant risk or investigational device exemption studies and post-market clinical follow-up studies, taking personal accountability for ethical conduct, regulatory compliance, and scientific integrity of assigned studies; operational execution of all study phases is managed by Clinical Operations.
  • Maintain current Good Clinical Practice certification and working knowledge of FDA investigational device exemption regulations (21 CFR Part 812), Institutional Review Board submission requirements, and informed consent obligations; serve as Principal Investigator signatory and primary medical point of contact for Institutional Review Boards, ethics committees, and regulatory bodies on study conduct, protocol amendments, and safety reporting obligations.
  • Provide medical direction to Clinical Operations on study design, protocol intent, and clinical judgment throughout study conduct; review and interpret interim and final study data, provide medical assessment of safety signals and adverse events, and escalate findings appropriately to Regulatory Affairs and Quality.
  • Provide medical review and Principal Investigator sign-off on clinical study reports prepared by Clinical Operations; collaborate with Evidence Strategy & Scientific Communications to initiate the publication process upon report completion.
  • Develop and deliver medical and clinical education programs for internal teams, including Sales, Marketing, Customer Experience, and Product Development, to build organizational understanding of relevant clinical topics, disease states, and patient populations.
  • Serve as an internal educator on pediatric health, infant monitoring, respiratory and cardiac physiology, and the clinical context in which Owlet's products are used.
  • Create and maintain internal medical reference materials, clinical frequently asked questions, and training content to support accurate and compliant communication across teams.
  • Provide medical and clinical input into commercial strategy, including product positioning, indication framing, and healthcare-provider-facing value propositions for the prescription device and over-the-counter/wellness product.
  • Serve as medical approval authority for customer-facing promotional materials, digital content, and advertising; participate in medical-legal-regulatory review and ensure scientific accuracy and regulatory compliance across all channels.
  • Support Sales with clinical materials, healthcare-provider objection-handling content, and medical education resources; participate in key customer or payer discussions as the medical representative when needed.
  • Collaborate with Marketing on evidence-based messaging frameworks and consumer scientific communications for the over-the-counter/wellness product, ensuring claims are defensible under FDA and Federal Trade Commission standards.
  • Serve as an external clinical voice for Owlet by engaging healthcare providers, pediatricians, neonatologists, and other clinical stakeholders in scientific and medical exchange.
  • Build and manage relationships with key opinion leaders and clinical advisors; plan and facilitate advisory board meetings and steering committees.
  • Represent Owlet at medical conferences, professional society meetings, and educational events; deliver presentations and participate in scientific exchange activities.
  • Lead development of healthcare-provider-facing medical education materials, clinical evidence summaries, and external-facing white papers in collaboration with Evidence Strategy & Scientific Communications.
  • Support media and public relations activities requiring medical expertise and clinical credibility, including consumer health messaging and press inquiries involving medical claims.
  • Identify and surface external research opportunities, including investigator-initiated studies, academic collaborations, and registry partnerships, through key opinion leader and advisory relationships; communicate these opportunities to Evidence Strategy & Scientific Communications to inform the evidence roadmap and integrated publication plan.
  • Contribute clinical content to regulatory submissions and filings, including 510(k), De Novo, or premarket approval applications, by providing medical narrative, risk-benefit assessment, and clinical interpretation; support predicate identification and equivalence analyses in collaboration with Regulatory Affairs.
  • Review labeling, instructions for use, and other product documents for clinical accuracy; collaborate with Evidence Strategy & Scientific Communications to align medical affairs priorities with the publication and evidence agenda.
  • Provide medical input to Product Development during design and post-market phases, including voice-of-customer activities, clinical use case definition, and contribution to artificial-intelligence-enabled product and data workflows such as algorithm design input, clinical validation of model outputs, and review of AI-driven features intended to improve infant safety, health, and sleep.
  • Serve as a clinical thought partner to Data Science and Product teams, ensuring data models, AI outputs, and product features are clinically meaningful, appropriately evidenced, and aligned with pediatric care standards.
  • Track scientific and clinical developments, healthcare delivery trends, and competitive intelligence relevant to Owlet's product portfolio and evidence priorities.

Desired Qualifications

  • Familiarity with infant monitoring, cardiorespiratory physiology, pulse oximetry, or pediatric sleep medicine.
  • Good Clinical Practice certification or willingness to obtain it before clinical study initiation; working knowledge of FDA investigational device exemption regulations (21 CFR Part 812) and Institutional Review Board processes is a plus.
  • Experience in a consumer health or over-the-counter product context.
  • Prior startup or early-stage company experience.

About the Company

Owlet

Wearable infant health monitor and sleep

Owlet Care makes infant health monitoring devices and sleep improvement tools. Its main product is the Smart Sock, a wearable that tracks an infant's heart rate, oxygen levels, and sleep patterns and sends the data to a mobile app so parents can monitor their baby in real time. It also offers the Dream Lab, a personalized sleep training program to help improve baby sleep habits. The company sells directly to consumers and through retail partners, generating revenue from Smart Sock devices, Dream Lab programs, accessories, extended warranties, and a subscription that unlocks advanced features and insights in the app. Compared to other baby tech options, Owlet combines continuous health monitoring with a structured sleep-training program and a subscription model, targeting new parents seeking peace of mind. Its goal is to provide reliable health data and practical sleep guidance to help parents care for their baby’s well-being.

Company size
201-500
Company stage
IPO
Headquarters
Lehi, UT
Founded
2013

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