myTomorrows

Health Tech

RegulatoryAffairsDirector

€130–195k ~AI est. Amsterdam, Netherlands FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Director candidates.

The Brief

“Regulatory Affairs Director at myTomorrows. Translate company and RA/PV strategy into regulatory plans. Drive implementation across EAPs”

Industry & Context.

Health Tech

What They're Looking For.

Must Have

Significant experience in Regulatory Affairs, Experience in pharma, biotech, or CRO, Proven experience managing multiple programs, Proven experience managing complex regulatory portfolios, Knowledge of global regulatory frameworks, Demonstrated leadership experience managing teams, Demonstrated experience developing talent

What You'll Do.

Translate company and RA/PV strategy into regulatory plans

Drive implementation across EAPs

Drive implementation across Clinical Trials

Drive implementation across Real-World Data initiatives

Oversee multiple regulatory programs

Ensure delivery against timelines

Ensure delivery against quality standards

Ensure delivery against client expectations

Identify and manage cross-program risks

Identify and manage dependencies

Identify and manage resource constraints

Lead Regulatory Affairs Managers

Coach Regulatory Affairs Managers

Develop Regulatory Affairs Managers

Lead senior team members

Coach senior team members

Develop senior team members

Set clear expectations for performance

Drive accountability for performance

Set clear expectations for quality

Drive accountability for quality

Set clear expectations for delivery

Drive accountability for delivery

Partner with Program Management

Partner with Medical Affairs

Partner with Quality Assurance

Partner with Supply Chain

Ensure regulatory input is embedded

Drive standardization of regulatory processes

Drive consistency of regulatory processes

Drive scalability of regulatory processes

Identify improvement opportunities

Implement data-driven solutions

Act as senior point of contact for clients

Support client discussions

Support regulatory interactions with Health Authorities

Ensure adherence to global regulatory requirements

Ensure adherence to internal processes

Support inspection readiness

Support audit preparedness

How You'll Work.

Team & Collaboration

Cross-functional teams; Program Management; Medical Affairs; Quality Assurance; Supply Chain

Communication Scope

Stakeholder management

Process & Methodology

Program management

Full Job Description

About myTomorrows  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.  THE OPPORTUNITY: REGULATORY AFFAIRS DIRECTOR 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. WHAT YOU'LL DO IN THIS ROLE: DRIVE REGULATORY STRATEGY

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