Compliance Counsel

About my Tomorrows

my Tomorrows is a global health tech company dedicated to breaking down barriers for patients seeking treatment options.

We strive to enable earlier and better treatment access by bridging the gap between those searching for possible options,and the companies whodevelopthem. We work closely with patients, healthcare professionals, trial sites, patient advocacy groups, and Bio Pharma – connecting key stakeholders in the drug development ecosystem.

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.

With a global footprint spanning 134 countries, to date we’ve supported over 17,000 patients, 2,900 physicians and 350 sites, earning the trust of 50+ Bio Pharma companies. In October 2025, we closed a €25M investment with Avego Healthcare Capital to fuel our global ambitions and scale the business.

Join us in shaping the future of treatment access - making tomorrow’s therapies accessible for people who need them today.

As our Compliance Counsel, you will help evolve and scale my Tomorrows’ global Compliance function. You will be responsible for further building a comprehensive compliance framework that supports our growing activities with patients, HCPs, PAGs and healthcare institutions, and for enabling compliant expansion of our Global Access initiatives. You will work closely with Medical Operations, Commercial, and Quality teams to ensure that compliance is embedded in daily operations.

This role sits within our Legal & Compliance team and reports to the General Counsel.

• Serve as a subject‑matter expert on global healthcare compliance, including GxP, anti‑kickback laws, anti‑bribery/anti‑corruption, and sanctions requirements.

• Lead the next phase of our healthcare compliance framework: define and strengthen rules and processes governing interactions with patients, HCPs, patient advocacy groups, and healthcare partners.

• Build and support a structured governance framework for local Medical Affairs and MSL activities as we scale our Global Access capabilities.

• Finetune our company‑wide process for third‑party and counter party screening, including sanctions, ABAC, and reputational checks.

• Manage core compliance operations, including risk assessments, monitoring, reporting mechanisms, and continuous improvement of controls.

• Conduct healthcare compliance review of commercial and medical materials, and assess collaborations to ensure compliant communication and engagement.

• Review and update internal policies, SOPs, guidance documents, and training materials; ensure alignment with current regulations and practical use by teams.

• Provide guidance on compliance considerations across clinical trial recruitment, Expanded Access Programs, RWD/RWE activities, and Bio Pharma partnerships.

• Support compliance incident management, including investigations, documentation, root‑cause analysis, and corrective actions.

• Monitor regulatory developments across key regions and translate them into clear, actionable guidance for internal teams.

• Engage with external counsel and regulators when required.

• Contribute to a culture of ethical behavior, sound decision‑making, and responsible innovation.

• Law degree and bar qualification in the EU, UK, or US

• 6+ years of experience in healthcare, pharmaceutical, life sciences, or health‑tech compliance

• Strong understanding of global healthcare regulations and familiarity with FDA/EMA or comparable authorities

• Experience working with Medical Affairs, Clinical Operations, Market Access, and Commercial teams

• Experience building or improving compliance frameworks, especially around HCP/patient engagements or third‑party screening

• Ability to work pragmatically in a fast‑moving, international environment with evolving processes

• Clear, concise communication skills and ability to translate regulations into…