Senior Legal Counsel, Product, AI & US

<p><strong>About myTomorrows</strong> </p><p>myTomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options.   </p><p>We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options, and the companies who develop them. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and BioPharma – connecting key stakeholders in the drug development ecosystem.   </p><p>We’ve developed a cutting-edge AI-powered technology platform that simplifies and streamlines access to drugs in development. To support our users and clients, we have a range of industry-expert specialized teams ready to help. Our services include clinical trial patient recruitment, Expanded Access Program management and Real-World Data collection.   </p><p>With a global footprint spanning 125 countries, to date, we’ve supported over 15,000 patients and 2,400 physicians, earning the trust of 50+ Biopharma companies.   </p><p>Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today. </p><p><strong>The opportunity: Senior Legal Counsel, Product, AI &amp; US</strong></p><p>This role is focused on enabling scalable platform development, AI governance, and healthcare compliance integration. You will provide the strategic product legal input to ensure our market (US and ex-US) expansion and product offerings are built on a sound regulatory foundation.</p><p><strong>What you'll do in this role: </strong></p><ul><li><p>Product &amp; Platform development</p><ul><li><p>Partner with Product and Engineering teams to design compliant SaaS, subscription, and platform models.</p></li><li><p>Define allocation of regulatory and compliance risks across product tiers (free, subscription, enterprise).</p></li><li><p>Anticipate legal and regulatory challenges in product development and build preventive frameworks.</p></li></ul></li><li><p>US Healthcare Regulatory expertise</p><ul><li><p>Lead on US healthcare regulatory matters (HIPAA, telehealth, state-specific rules).</p></li><li><p>Provide strategic guidance on US-specific risks and requirements to enable product and business growth.</p></li></ul></li><li><p>AI Governance &amp; enablement</p><ul><li><p>Own company-wide AI governance framework, including policies, risk assessments, and regulatory monitoring.</p></li><li><p>Partner with product, data, and compliance teams to ensure AI systems comply with ethical, legal, and healthcare regulatory standards.</p></li><li><p>Promote safe, transparent, and compliant AI adoption across business functions, enabling innovation while managing risk.</p></li></ul></li><li><p>Contracting (strategic input)</p><ul><li><p>Define contractual frameworks that support platform scalability.</p></li><li><p>Partner with Privacy &amp; Contracting Counsel (execution owner) to ensure US-specific requirements are embedded into templates and playbooks.</p></li><li><p>Provide oversight for high-value or high-risk strategic partnerships.</p></li></ul></li><li><p>Knowledge contribution</p><ul><li><p>Bring working knowledge of (observational) study designs, clinical trial frameworks, and healthcare research regulations to strengthen team capabilities.</p></li><li><p>Support Compliance &amp; Risk Counsel in spotting potential overlaps between healthcare compliance, product use cases, and study design considerations.</p></li></ul></li><li><p>Cross-functional collaboration</p><ul><li><p>Act as the bridge between product, compliance, and commercial functions for regulatory integration.</p></li><li><p>Ensure global alignment between US and EMEA legal approaches.</p></li></ul></li></ul><p> </p><p><strong>What you bring to the table: </strong></p><ul><li><p>Qualified lawyer in the EU with demonstrable US healthcare law expertise and/or JD from an accredited law school; admitted to practice in at least one US state.</p></li><li><p>8+ years’ legal experience, ideally in healthtech/medtech/SaaS, with strong in-house exposure.</p></li><li><p>Demonstrated success in supporting product development.</p></li><li><p>Expertise in US healthcare laws and risk allocation in regulated industries.</p></li><li><p>Ability to work autonomously and cross-functionally in a fast-paced, global environment.</p></li><li><p>Familiarity experience balancing healthcare regulations with SaaS or platform risk allocation.</p></li><li><p>Strong ability to translate complex regulations into actionable product requirements.</p></li><li><p>Familiarity with clinical trial regulations.</p></li></ul><p> </p><p><strong>What success in the first 12 months looks like: </strong></p><ul><li><p>Platform clarity: Deliver a product-focused platform legal framework based on upcoming and expected legal and regulatory trends for a global platform</p></li><li><p>AI Governance &amp; adoption: Deliver a practical AI governance framework and driv