myTomorrows

Biotech

RegulatoryAffairsDirector

€135–195k ~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. Skills: Regulatory strategy, Program oversight, Team leadership. Drive regulatory strategy execution. Translate strategy into plans”

Industry & Context.

Biotech
Problems you'll solve

Risk management

What They're Looking For.

Must Have

Advanced degree life sciences, Significant experience Regulatory Affairs, Experience managing multiple programs

What You'll Do.

Drive regulatory strategy execution

Translate strategy into plans

Drive implementation across EAPs

Oversee program delivery

Ensure delivery against timelines

Identify and manage risks

Set clear expectations

Drive accountability for performance

Partner with cross-functional teams

Ensure regulatory input embedded

Drive standardization of processes

Identify improvement opportunities

Implement data-driven solutions

Act as senior point of contact

Support client discussions

Support regulatory interactions

Ensure adherence to requirements

Ensure adherence to processes

Support inspection readiness

Support audit preparedness

How You'll Work.

Team & Collaboration

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

Communication Scope

Client discussions; Health Authority interactions

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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