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.
Hippocratic AI is rapidly expanding across the pharma and medtech industries. We are building a new class of agentic AI that supports patients and healthcare stakeholders across the entire life sciences value chain including patient services, clinical trials, access, adherence, and HCP-facing workflows. We are contracted with 5 of the top 20 pharma globally and are in a hyper growth phase for our Life Sciences vertical.
Backed by the world’s leading Life Science 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.
We are seeking a Head of Medical Affairs & Regulatory to lead the integrated medical and regulatory strategy for our AI-powered healthcare platform. This executive will define how Hippocratic AI operates credibly and compliantly across pharma, medtech, diagnostics, provider systems, and global regulatory environments. You will serve as the senior authority on medical governance, MLR frameworks, regulatory positioning, and compliant AI deployment.
This role sits at the intersection of innovation and oversight — ensuring we move quickly while maintaining the highest standards of scientific integrity, regulatory compliance, and patient safety. The ideal candidate understands pharma operations end-to-end and can create clarity and structure in highly dynamic, ambiguous environments. Join experts who’ve spent their careers improving care, advancing science, and building world‑changing technologies — ensuring our platform is powerful, trusted, and truly transformative.
The Head of Medical Affairs and Regulatory is responsible for ensuring Hippocratic AI's life sciences platform meets the scientific, medical, and regulatory standards required to operate within life science environments. You will serve as the company's authoritative voice on medical accuracy, regulatory compliance, adverse event handling, and non-promotional engagement standards — working at the intersection of product, customer deployments, and external stakeholders.
You will guide how the platform handles medical information, safety signals, MLR review processes, and regulatory requirements across therapeutic areas and geographies. You will also support enterprise sales and deployment conversations where medical credibility and regulatory confidence are critical to closing and scaling accounts.
You will report to the President of Life Sciences, and work closely with Sales, Customer Success, Product, and Engineering leadership.
What We're Looking For
A medical and regulatory leader who can establish Hippocratic AI as a trusted, compliant platform in the eyes of pharma's most rigorous stakeholders. A hands-on operator who builds frameworks and processes rather than waiting for them to exist. A customer-facing expert who gives pharma executives confidence that the platform meets the highest standards for safety, accuracy, and regulatory compliance. A strategic thinker who understands that regulatory credibility is a competitive advantage and a prerequisite for scaling in life sciences. A builder who wants to define how AI-enabled patient engagement is governed during a transformative period in the industry.
Key Responsibilities
Medical Affairs Strategy and Oversight
Define and maintain the medical and scientific standards that govern the platform's patient-facing and HCP-facing interactions.
Establish frameworks for medical information delivery, ensuring responses are accurate, evidence-based, and aligned with approved labeling and non-promotional requirements.
Advise on the platform's handling of medical inquiries, off-label questions, and clinical content across therapeutic areas.
Creative thinker who brings original ideas to the table and can partner with the product team to architect purpose-built AI agents for medical affairs workflows
Partner with Product and Engineering to embed medical guardrails, escalation pathways, and clinical logic into platform workflows.
Stay current on therapeutic landscape developments, treatment guidelines, and medical communication best practices relevant to the platform's use cases.
Regulatory and Compliance Guidance
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.
Enterprise Sales and Deployment Support
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.
Scaling and Knowledge Development
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 perspectives on commercial model transformation, patient services evolution, and the strategic implications of agentic AI for pharma operating models.
Build internal knowledge bases covering AE reporting workflows, MLR requirements, non-promotional standards, and therapeutic areas–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.
Qualifications
Required
7–15 years of experience in medical affairs, pharmacovigilance, regulatory affairs, or drug safety within pharma, biotech, or life sciences services organizations.
Deep working knowledge of adverse event reporting, pharmacovigilance regulations, MLR review processes, non-promotional communication standards, and medical information operations.
Strong understanding of FDA and EMA regulatory frameworks as they apply to patient engagement, medical communications, and digital health technologies.
Demonstrated 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 high expectations for ownership and cross-functional collaboration.
Exceptional written and verbal communication skills.
Preferred
Experience with digital health platforms, AI in healthcare, or patient engagement technologies.
Familiarity with HIPAA, GDPR, and data privacy frameworks in the cont
Hippocratic%20ai
https://hippocratic%20ai.com