Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Head of Regulatory Affairs

Hippocratic AI

About Us

Hippocratic AI is the leading generative AI company in healthcare. We have the only system that can have safe, autonomous, clinical conversations with patients. We have trained our own LLMs as part of our Polaris constellation, resulting in a system with over 99.9% accuracy.

Why Join Our Team

Reinvent healthcare with AI that puts safety first. We're building the world's first healthcareonly, safetyfocused LLM - a breakthrough platform designed to transform patient outcomes at a global scale. This is category creation.

Work with the people shaping the future. Hippocratic AI was cofounded by CEO Munjal Shah and a team of physicians, hospital leaders, AI pioneers, and researchers from institutions like El Camino Health, Johns Hopkins, Washington University in St. Louis, Stanford, Google, Meta, Microsoft, and NVIDIA.

Backed by the world's leading healthcare and AI investors. We recently raised a $126M Series C at a $3.5B valuation, led by Avenir Growth, bringing total funding to $404M with participation from CapitalG, General Catalyst, a16z, Kleiner Perkins, Premji Invest, UHS, Cincinnati Children's, WellSpan Health, John Doerr, Rick Klausner, and others.

Build alongside the best in healthcare and AI. Join experts who've spent their careers improving care, advancing science, and building worldchanging technologies - ensuring our platform is powerful, trusted, and truly transformative.

Location Requirement

We believe the best ideas happen together. To support fast collaboration and a strong team culture, this role is expected to be in our Menlo Park office five days a week, unless otherwise specified.

About the Role

The Head of Regulatory Affairs is responsible for leading and executing global and domestic regulatory strategy, filings, and compliance activities for (a) clinical trials for pharmaceuticals, biologics, and medical devices, and (b) AI-driven SaMD products. This role requires a practitioner who not only knows FDA culture and regulatory frameworks, but can also operationalize them, drafting documents, building processes, and coordinating cross-functional activities. Successful candidates will be able to interface with our customer's regulatory leads to ensure alignment and successful deployment of our AI in the pharma and medtech space. This role will work closely with our legal, pharma, clinical, and IT teams.

What You'll Do
Regulatory Strategy & Execution
  • Help develop and support regulatory strategies and submissions for AI-enabled SaMD products, including classification, marketing applications (e.g., NDAs, De Novo, 510(k)), and pre-submission pathways.
  • Help develop and support regulatory documentation that enables our customers in the pharma and medtech space to meet their compliance obligations when using Hippocratic AI's products.
  • Lead hands-on preparation of regulatory submissions with Legal: drafting sections, coordinating data inputs, managing timelines, and ensuring high-quality documentation.
  • Translate regulatory requirements into specific, actionable tasks for clinical, product, engineering, and quality teams.
  • Oversee and advance global and domestic regulatory and compliance initiatives, maintaining scientific accuracy, proactively managing risk, and keeping the organization aligned with changing regulatory expectations.
Regulatory Compliance
  • Build, manage, and continuously improve a practical regulatory compliance structure across SaMD development lifecycles.
  • Collaborate with legal, engineering, clinical, product, and quality teams to ensure compliance with applicable regulations, including 21 CFR Parts 210 and 211, 21 CFR Part 820, SaMD guidance, AI/ML-specific expectations and guidance, cybersecurity, and labeling requirements.
  • Help design, support, and maintain a compliant regulatory framework and Pharma-partner guidelines, including iterative AI development, model updates, QMS and GMP requirements, audits and inspections, real-world performance, and post-market monitoring and mitigation.
  • Develop and maintain SOPs, controlled documents, audit readiness materials, and inspection response processes.
  • Stay ahead of evolving regulatory policies and draft internal guidance to translate new requirements into clear action for cross-functional teams.
  • Interact with customer regulatory leads to facilitate deployment of Hippocratic's solutions with customers in the pharma and medtech industry.
Cross-Functional Leadership
  • Partner with legal, product, and engineering teams during development to define regulatory requirements early and de-risk product strategy.
  • Educate technical and clinical teams on regulatory expectations, FDA and pharmaceutical industry norms, and quality documentation needs.
  • Drive internal regulatory training and ensure that cross-functional teams have clear guidance, templates, timelines, and expectations.
  • Bring creative, practical solutions to regulatory challenges inherent in AI technology in the healthcare space.
Innovation & Process Building
  • Build lightweight regulatory processes appropriate for a startup environment without sacrificing compliance.
  • Use regulatory knowledge to enable innovation, not block it - finding pathways that support speed, safety, and responsible AI.
  • Identify gaps in regulatory readiness and implement corrective actions proactively.
  • Contribute to internal playbooks, templates, and scalable processes across regulatory and compliance functions.
What You Bring
Must-Have:
  • 10-12 years of regulatory affairs experience spanning medical devices, digital health, pharmaceuticals, and related FDA-regulated products.
  • Bachelor's degree in life science required.
  • Experience working at the FDA or directly interfacing extensively with FDA. Strong experience with FDA regulations and regulatory landscape.
  • Strong understanding of industry, including clinical trials, drug and device development, patient support services, ad/promo, pharmacovigilance, and post-market activities
  • Demonstrated experience preparing and submitting INDs, NDAs/BLAs, 510(k)s, De Novos, PMAs, supplements, and/or Q-subs.
  • Strong experience with drug, device, and SaMD development, submissions, and regulatory pathways.
  • Familiarity with AI-enabled medical technologies, machine learning considerations, and evolving FDA expectations for AI/ML.
  • Demonstrated ability to thrive in fast-paced, dynamic startup environments with limited structure and high ownership.
  • Excellent written and verbal communication skills, especially for FDA submissions and internal education.
Nice-to Have:
  • Experience working in a startup or emerging-growth private company.
  • Prior leadership experience building regulatory frameworks or managing cross-functional initiatives.
  • PhD, PharmD or Master's degree preferred. RAC certification or equivalent is a plus.
What We're Looking For
  • A regulatory leader who combines strategic thinking with detailed operational follow-through.
  • Someone who respects regulatory structure but is creative, innovative, and solutions-oriented.
  • A builder who wants to create the regulatory foundation for both advanced AI systems and traditional drug/device programs.
  • A collaborator who can work seamlessly with clinical, technical, product, and executive teams.

Please be aware of recruitment scams impersonating Hippocratic AI. All recruiting communication will come from @hippocraticai.com email addresses. We will never request payment or sensitive personal information during the hiring process.
Why Join Hippocratic AI

Reinvent healthcare with AI that puts safety first. We're building the world's first healthcareonly, safetyfocused LLM - a breakthrough platform designed to transform patient outcomes at a global scale. This is category creation.

Work with the people shaping the future. Hippocratic AI was cofounded by CEO Munjal Shah and a team of physicians, hospital leaders, AI pioneers, and researchers from institutions like El Camino Health, Johns Hopkins, Washington University in St. Louis, Stanford, Google, Meta, Microsoft, and NVIDIA.

Backed by the world's leading healthcare and AI investors. We recently raised a $126M Series C at a $3.5B valuation, led by Avenir Growth, bringing total funding to $404M with participation from CapitalG, General Catalyst, a16z, Kleiner Perkins, Premji Invest, UHS, Cincinnati Children's, WellSpan Health, John Doerr, Rick Klausner, and others.

Build alongside the best in healthcare and AI. Join experts who've spent their careers improving care, advancing science, and building worldchanging technologies - ensuring our platform is powerful, trusted, and truly transformative.
Equal Opportunity

Hippocratic AI is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, national origin, sex, age, disability, sexual orientation, gender identity or expression, genetic information, military or veteran status, or any other characteristic protected by applicable law. We are committed to building a team that reflects the patients we serve. We actively encourage applications from candidates of all backgrounds. If you require accommodations during the hiring process, please contact View email address on click.appcast.io.

Please be aware of recruitment scams impersonating Hippocratic AI. All recruiting communication will come from @ hippocraticai.com email addresses. We will never request payment or sensitive personal information during the hiring process.
Vacancy posted 4 days ago
Similar jobs that could be interesting for youBased on the Head of Regulatory Affairs in Menlo Park, CA vacancy
  • $250k - $300k

    Menlo Park, CARegulatory Affairs - Regulatory Affairs /Regular, Full-Time Employee /On-siteMore than one million people in the United States today...  ...Senior Director, Regulatory Affairs is Orca Bio's functional Head of Regulatory Affairs, leading the Regulatory Affairs... 
    Suggested
    Full time
    Local area
    Immediate start
    Remote work

    Orca Bio

    Menlo Park, CA
    4 days ago
  • $302.01k - $390.83k

     ...help create possible, together.Job DescriptionJOB DESCRIPTIONLead CMC teams/ groups to support the CMC product and portfolio regulatory affairs goals and contribute to the development of global regulatory initiatives.Lead global CMC regulatory strategies, including risk... 
    Suggested
    Full time
    For contractors
    Local area

    GILEAD Sciences

    Foster, CA
    2 days ago
  • $200k - $250k

     ...of compliance risk across all business lines and legal entities.The CCO provides strategic leadership across Consumer Compliance, Regulatory Compliance, and BSA/AML Compliance while partnering closely with Product, Operations, Technology, Legal, Finance, and Internal... 
    Suggested
    Flexible hours

    Taba Pay Inc

    Palo Alto, CA
    1 day ago
  •  ...global AI and digital health company. They operate as an equal opportunity employer. About the role: The Head of Quality Engineering & Regulatory Affairs (Head of QERA) is a key executive reporting to the Chief Product Officer, responsible for building, leading... 
    Suggested
    H1b
    Remote work
    Worldwide

    Stirling QR

    Menlo Park, CA
    13 days ago
  • $340k - $370k

    The VP of Regulatory and Head of Regulatory Affairs will shape and execute regulatory strategies and lead and manage submissions to support clinical development and regulatory compliance for Sagimet. This role will serve as the primary liaison with global regulatory authorities... 
    Suggested

    Sagimet Biosciences

    Foster, CA
    23 hours ago
  • $191k - $252k

     ...issues management, governance and management reporting, and metrics.Our department prevents, detects and mitigates compliance and regulatory risks across the firm and helps to strengthen our culture of compliance. As a company involved in digital assets, this role will... 
    Full time
    Local area
    Relocation package

    FalconX

    San Mateo, CA
    1 day ago
  •  ...with active membership in a Bar Association or equivalent body. International experience and a deep understanding of the global regulatory landscape, particularly in key markets such as the US, China, Europe, and Japan, are essential. The role requires a leader with therapeutic... 

    Confidential

    Foster, CA
    3 days ago
  • $153k - $178k

     ...performing method development, supporting method transfer, and executing various characterization testing activities that enable regulatory filings. This role will serve as the primary compliance partner for the AD laboratories, working collaboratively with Quality Assurance... 
    Work experience placement

    Vaxcyte

    San Carlos, CA
    23 hours ago
  • $244k - $305k

     ...Serve as the strategic compliance advisor to Commercial, Medical Affairs, Market Access, Patient Services, and other field-facing...  ...improvements, technology implementations, and evolving legal or regulatory requirements.The successful candidate will demonstrate flexibility... 
    Full time
    Local area
    Shift work

    Revolution Medicines

    Redwood City, CA
    2 days ago
  • $129.5k - $175k

     ...and maintain relationshipsWork across multiple frameworks and regulatory standards, including but not limited to ISO, PCI, NIST, AICPA SOCDrive...  ...workforce that reflects the world we live in.If you are head-over-heels about this role but unsure if you meet all the requirements... 
    Live in
    Work at office
    Shift work
    3 days per week

    Box

    Redwood City, CA
    4 days ago
  • $183k - $194k

     ...activities. This role develops and executes multi-product global regulatory CMC strategies for investigational products and leads the...  ...changing regulations.Essential Functions:Represent Regulatory Affairs in various internal cross-functional project teams, improvement... 
    Relocation
    Relocation package

    Vaxcyte

    San Carlos, CA
    3 days ago
  •  ...A biopharmaceutical company in Redwood City is seeking an Executive Director of Regulatory Affairs CMC to lead the regulatory strategy for drug products. The ideal candidate will have 15 years of regulatory CMC experience and a successful track record in preparing BLAs... 

    Allakos Inc

    Redwood City, CA
    1 day ago
  • Corcept Therapeutics is seeking a Director-level Regulatory Medical Writer to lead strategic medical writing for NDA submissions and regulatory documents in a fast-paced, small company environment. You will manage a team and external vendors, define content standards,... 

    Corcept Therapeutics

    Redwood City, CA
    4 days ago
  • El Camino Health is seeking a Director Accreditation, Regulatory & Licensure to lead regulatory readiness across the organization, ensuring compliance with Joint Commission, CMS CoPs, California Title 22, and CDPH regulations. The role collaborates with executives, service... 

    El Camino Health

    Mountain View, CA
    2 days ago
  • About Workato Workato delivers enterprise infrastructure for the agentic era, redefining iPaaS and helping enterprises unify data, applications, processes, and AI into a single, governed platform. A leader in Enterprise MCP and trusted by 50% of the Fortune 500, Workato...
    Remote work
    Flexible hours

    Workato

    Palo Alto, CA
    1 day ago
  • $211k - $264k

     ...tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.The Opportunity:The Director of Regulatory Affairs (US Filing Lead) is accountable for driving preparation & execution of Regulatory NDA/MAA filings for late-stage oncology... 
    Full time
    Work experience placement
    Local area

    Revolution Medicines

    Redwood City, CA
    23 hours ago
  • $244k - $305k

     ...Opportunity:The Senior Director, Molecule Global Regulatory Lead will develop and execute global...  ...growth. The position reports to the Head of Regulatory Sciences and serves as a key...  ...considered.Approximately 12+ years of regulatory affairs experience within the biotechnology or... 
    Full time
    Local area

    Revolution Medicines

    Redwood City, CA
    2 days ago
  • $130k - $179k

     ...Manager, Regulatory Affairs Redwood City, CA JOIN US! Adicet Bio, Inc. is a clinical stage biotechnology company discovering and developing allogeneic gamma delta T cell therapies for autoimmune diseases and cancer. Adicet is advancing a pipeline of "off-the-shelf... 
    Full time
    Temporary work
    Work at office
    Flexible hours
    3 days per week

    Adicet Bio, Inc

    Redwood City, CA
    23 hours ago
  •  ...therapy, including gene‑edited cell therapy, which may be a promising option for patients with cancer. Overview The Manager, Regulatory Affairs, represents Regulatory Affairs on cross‑functional teams, working closely with other team members to support corporate and departmental... 
    Work at office
    Remote work

    Iovance Biotherapeutics, Inc.

    San Carlos, CA
    3 days ago
  •  ...risk assessments, audit preparation, and ongoing compliance initiatives.Maintain documentation related to cybersecurity, governance, risk, and compliance programs.Support regulatory and industry framework initiatives, including HIPAA, NIST, SOC, and related standards.

    Robert Half

    Redwood City, CA
    2 days ago
  •  ...management of CHC’s enterprise-wide compliance program. The Compliance Director will ensure CHC maintains rigorous standards for regulatory compliance and continuous quality improvement through regular audits, incident metrics, corrective action tracking, and staff training... 
    Full time
    Work at office
    Local area

    Page Mechanical Group Inc

    Palo Alto, CA
    2 days ago
  • $166k - $195k

     ...demonstrating integrity, accountability, equality and clarity across communications and decision making.Summary:The Sr. Project Manager, Regulatory CMC will serve as a key contributor to the company’s project management, regulatory and CMC functions. Reporting to the Vice... 
    3 days per week

    Vaxcyte

    San Carlos, CA
    23 hours ago
  • $186k - $233k

     ...insights, audit findings, industry trends, enforcement actions, and regulatory developments.Serve as a senior presenter and facilitator for...  ....Significant experience supporting Commercial and Medical Affairs organizations in a biopharmaceutical environment.Demonstrated... 
    Full time
    Local area

    Revolution Medicines

    Redwood City, CA
    4 days ago
  •  ...lifespan.   We’re hiring an experienced new member of our Regulatory team who will own the strategy and operations for our Chemistry...  ...work. As one of the earliest members of the Regulatory Affairs team, you will work across Retro’s programs and play a leading... 

    Retro

    Redwood City, CA
    6 days ago
  • $180k - $210.5k

     ...activities. This role develops and executes multi-product global regulatory CMC strategies for investigational products and leads the...  ...scientific discipline (e.g. Biology, Chemistry, Pharmacy, Regulatory Affairs for Drugs, Biologics or Medical Devices). Minimum 10 years of... 

    Vaxcyte

    San Carlos, CA
    1 day ago
  • $164k - $205k

     ...activities throughout the system lifecycle, and partnering with Quality and business stakeholders to maintain inspection readiness and regulatory compliance. This position reports to the Sr. Director, IS Quality, Risk & Compliance.Responsibilities:Act as the Information... 
    Full time
    Local area

    Revolution Medicines

    Redwood City, CA
    23 hours ago
  •  ...with insulin-secreting tumors and related neuro-oncology disorders. Position Summary Reporting to the Chief Regulatory Officer, the Sr Director of Regulatory Affairs will join the regulatory team providing strategic and operational leadership supporting late-stage... 
    Local area

    Rezolute, Inc.

    Redwood City, CA
    1 day ago
  • Rezolute is seeking a Sr Director of Regulatory Affairs to lead regulatory strategy and execution for late-stage biologics programs. You will drive FDA interactions, strategy development, and submissions to support HI biology programs and tumor-related indications. This... 

    Rezolute

    Redwood City, CA
    2 days ago
  • Scorpion Therapeutics in Redwood City, CA, seeks a Sr Director of Regulatory Affairs to lead strategic and operational efforts for late-stage development, regulatory submissions, and U.S. registration. You will focus on FDA interactions and shaping global regulatory plans... 

    Scorpion Therapeutics

    Redwood City, CA
    4 days ago
  • $192.5k - $240.5k

    Why Box needs youBox is looking for a strategic events leader who can define how we show up in the market and ensure our event investments drive measurable business impact. This role is critical as we sharpen our strategy across marquee events, sponsored industry moments...

    Box

    Redwood City, CA
    21 hours ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Head of Regulatory Affairs. Be the first to apply!