
Job Overview
Location
Amsterdam HQ
Job Type
Full-time
Category
HR & Recruiting
Date Posted
April 22, 2026
Full Job Description
đź“‹ Description
- • The Director, Global Access at myTomorrows is a strategic leadership role responsible for shaping and executing global access strategies that enable compliant, sustainable patient access across international markets, bridging expanded access programs with post-marketing authorization readiness and ensuring alignment with reimbursement pathways and health system requirements.
- • Day to day, the role involves defining global access and post-MA readiness strategies, setting market sequencing priorities, designing access models and governance structures, overseeing distributor and Medical Science Liaison team build-out, ensuring CRM tracking and performance monitoring, partnering with Commercial, Legal, Compliance, and EAP Operations teams, and engaging with external stakeholders like governments and payors to support compliant access pathways.
- • myTomorrows is a global health tech company headquartered in Amsterdam with operations in 134 countries, dedicated to breaking down barriers for patients seeking treatment options by connecting patients, healthcare providers, trial sites, advocacy groups, and BioPharma companies through an AI-powered platform that streamlines access to drugs in development, having supported over 17,000 patients and earned the trust of 60+ BioPharma firms.
- • In this role, the person will develop deep expertise in global access strategy, regulatory compliance, and post-MA transition planning; build scalable, audit-ready access infrastructures; lead cross-functional initiatives that shape how the company prepares for commercialization; and establish trusted engagement models with health systems and partners that position myTomorrows as a benchmark for responsible, sustainable access enablement.
Skills & Technologies
About myTomorrows B.V.
myTomorrows B.V. operates an Amsterdam-based platform that connects physicians and patients worldwide with pre-approval and off-label medicines. The company identifies investigational or licensed drugs not yet commercially available in a patient’s country, navigates regulatory pathways, arranges supply, and supports pharmacovigilance. It serves oncology, neurology, and rare diseases, working with pharmaceutical companies, hospitals, and regulators in Europe, North America, and Asia-Pacific.
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