Regulatory Affairs Director

myTomorrows

17h

About The Position

myTomorrows 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 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. 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, 3,000 physicians and 350 sites, earning the trust of 60+ BioPharma 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 Regulatory Affairs Director, you will play a critical leadership role in translating our global regulatory strategy into execution across programs, regions, and service lines. You will oversee a portfolio of regulatory activities, ensuring high-quality, compliant, and timely delivery while leading and developing a team of Regulatory Affairs professionals. You’ll work closely with cross-functional teams and act as a senior point of contact for both internal stakeholders and external partners. This role sits at the intersection of strategy, delivery, and leadership, and is key to scaling our Regulatory Affairs capabilities globally.

Requirements

Advanced degree in life sciences, pharmacy, or a related field
Significant experience in Regulatory Affairs within pharma, biotech, or CRO environments
Proven experience managing multiple programs and complex regulatory portfolios
Strong knowledge of global regulatory frameworks (EAP, clinical trials, or similar environments)
Demonstrated leadership experience managing teams and developing talent
Excellent stakeholder management and communication skills

Responsibilities

Drive regulatory strategy execution
Translate company and RA/PV strategy into clear regulatory plans across programs and regions
Drive implementation across Expanded Access Programs (EAPs), Clinical Trials, and Real-World Data initiatives
Oversee program and portfolio delivery
Oversee multiple regulatory programs simultaneously, ensuring delivery against timelines, quality standards, and client expectations
Identify and proactively manage cross-program risks, dependencies, and resource constraints
Lead and develop the team
Lead, coach, and develop Regulatory Affairs Managers and senior team members
Set clear expectations and drive accountability for performance, quality, and delivery
Collaborate cross-functionally
Partner closely with Program Management, Medical Affairs, Quality Assurance, and Supply Chain
Ensure regulatory input is embedded into end-to-end program delivery
Drive operational excellence and performance
Drive standardization, consistency, and scalability of regulatory processes
Identify improvement opportunities and implement data-driven solutions
Engage with clients and stakeholders
Act as a senior point of contact for clients on regulatory matters
Support client discussions, audits, and regulatory interactions with Health Authorities
Ensure quality, compliance, and risk management
Ensure adherence to global regulatory requirements and internal processes
Support inspection readiness and audit preparedness