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Hippocratic AI

Licenses safety-focused healthcare LLMs to institutions

Medical Regulatory Lead

Biology & BiotechConfirmed live in the last 24 hours
Full-timeMenlo Park, CA, USANo salary listedIn-person

About the Job

Requirements

  • Seven to fifteen years of experience in regulatory operations or regulatory affairs within pharma, biotech, or life sciences services organizations.
  • Deep working knowledge of MLR review processes, non-promotional communication standards, medical information operations, adverse event reporting, and pharmacovigilance regulations.
  • Strong understanding of FDA and EMA regulatory frameworks as they apply to patient engagement, medical communications, and digital health technologies.
  • Ability to engage credibly with VP, SVP, and C-suite stakeholders across medical, regulatory, legal, and compliance functions at pharma organizations.
  • Experience translating regulatory and medical requirements into operational workflows, product requirements, or technology specifications.
  • Comfort working in high-growth environments with limited structure and ownership and cross-functional collaboration.
  • Written and verbal communication skills.

Responsibilities

  • Define and maintain regulatory standards that govern the platform's patient-facing and HCP-facing interactions.
  • Establish labeling operations frameworks for delivery, ensuring responses are accurate, evidence-based, and aligned with approved labeling and non-promotional requirements.
  • Advise on regulatory requirements to ensure the platform compliantly handles medical inquiries, off-label questions, and clinical content across therapeutic areas.
  • Partner with the product team to architect purpose-built AI agents for medical affairs workflows.
  • Partner with Product and Engineering to support medical guardrails, escalation pathways, and clinical logic in platform workflows.
  • Stay current on therapeutic landscape developments, treatment guidelines, and medical communication best practices relevant to the platform's use cases.
  • Own the regulatory strategy for how the platform operates within pharma customer environments, including MLR review processes, adverse event reporting obligations, and privacy requirements.
  • Guide internal teams and pharma customers on regulatory requirements across FDA, EMA, and other relevant jurisdictions as they apply to AI-enabled patient and HCP engagement.
  • Serve as the primary point of contact for customer medical, safety, legal, and regulatory stakeholders during sales and deployment conversations.
  • Partner with legal and compliance teams to ensure platform workflows meet HIPAA, GDPR, and industry-specific data governance standards.
  • Provide medical and regulatory credibility during enterprise sales conversations, RFP responses, and executive workshops with pharma customers.
  • Help Sales navigate MLR, pharmacovigilance, legal, compliance, and governance review processes within prospective and existing accounts.
  • Develop materials and frameworks that demonstrate the platform's regulatory readiness, safety architecture, and medical rigor to customer stakeholders.
  • Offer strategic oversight during early deployments to ensure medical accuracy, safety protocols, and compliance guardrails are properly configured and validated.
  • Translate learnings from customer engagements and pilot deployments into repeatable regulatory and medical affairs playbooks.
  • Develop and publish thought leadership on AI in pharma commercialization, including commercial model transformation, patient services evolution, and the strategic implications of agentic AI for pharma operating models.
  • Build internal knowledge bases covering adverse event reporting workflows, MLR requirements, non-promotional standards, and therapeutic-area-specific regulatory considerations.
  • Identify emerging regulatory trends in AI-enabled healthcare and patient engagement, and advise leadership on their implications for product and go-to-market strategy.

Desired Qualifications

  • Experience with digital health platforms, AI in healthcare, or patient engagement technologies.
  • Familiarity with HIPAA, GDPR, and data privacy frameworks in the context of patient-facing technology.
  • Prior experience supporting enterprise sales or technology deployments into large pharma organizations from a medical or regulatory perspective.
  • MD, PharmD, PhD, or an advanced scientific degree.
  • MBA, MPH, or MS.
  • Startup or early-stage company experience.

About the Company

Hippocratic AI

Licenses safety-focused healthcare LLMs to institutions

Hippocratic AI builds specialized language models for healthcare that hospitals and clinics license to support non-clinical tasks and improve patient care and operations. The models are trained on evidence-based medical content and refined with a Reinforcement Learning with Human Feedback process from healthcare professionals to ensure safety and reliability. It differentiates itself by prioritizing safety, equity, and bedside-appropriate interactions, with validation on healthcare exams to ensure real-world applicability. Its goal is to improve healthcare access, equity, and outcomes by providing safe, trustworthy AI tools for clinicians and patients.

Company size
201-500
Company stage
Series C
Total funding
$387M
Headquarters
Palo Alto, CA
Founded
2022

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