Job Overview
Location
Amsterdam HQ
Job Type
Full-time
Category
Writing
Date Posted
May 21, 2026
Full Job Description
đź“‹ Description
- • Lead the creation of long-form content including blogs, thought leadership pieces, case studies, and research-driven articles that translate complex clinical, regulatory, and drug development topics into clear, credible communication for patients, healthcare professionals, and BioPharma partners.
- • Adapt core messaging into fit-for-purpose copy across multiple channels: website, email campaigns, social media, promotional materials, and external publications while maintaining brand voice and factual integrity.
- • Translate highly technical inputs from internal subject matter experts — such as clinical trial protocols, Expanded Access Program details, and Real-World Data insights — into accurate, accessible, and engaging narratives without oversimplification or loss of authority.
- • Maintain exceptional editorial discipline in a regulated health-tech environment, ensuring all claims are evidence-based, compliant with industry standards, and review-ready for legal, medical, and compliance stakeholders.
- • Collaborate closely with cross-functional teams including clinical operations, medical affairs, product, and marketing to turn incomplete, fragmented, or ambiguous inputs into polished, coherent, and impactful content.
- • Utilize AI tools responsibly to enhance drafting speed, editing efficiency, and content repurposing, while preserving originality, voice, and factual accuracy — never substituting human judgment for clinical or regulatory precision.
- • Ensure all content aligns with myTomorrows’ mission to improve treatment access, reinforcing trust through transparency, empathy, and precision in language.
- • Apply consistent editorial standards across all outputs to create a recognizable, authoritative myTomorrows voice that reduces review cycles and increases stakeholder confidence.
- • Optimize content for SEO and AEO (Answer Engine Optimisation) to ensure visibility and relevance among patients and HCPs seeking information on clinical trials and expanded access pathways.
- • Deliver a steady pipeline of high-quality, audience-targeted content that directly supports patient recruitment, partner engagement, and brand credibility across 134 countries.
- • Analyze engagement metrics and audience insights to refine social copy, improve resonance, and inform future content strategy without compromising factual accuracy or regulatory compliance.
- • Serve as a content steward within the organization, setting benchmarks for clarity, tone, and compliance that elevate the overall quality of external communications.
- • Ensure all written materials reflect the company’s values of patient-centeredness, scientific rigor, and ethical responsibility in every word choice and claim.
- • Contribute to internal knowledge sharing by documenting best practices, creating content guidelines, and mentoring junior writers on navigating the complexities of health-tech communication.
- • Maintain up-to-date awareness of evolving regulatory landscapes in global clinical trial access, drug development pathways, and digital health communications to inform content strategy and risk mitigation.
🎯 Requirements
- • Proven experience and deep understanding of clinical trials, expanded access, drug development, or the BioPharma/health-tech landscape
- • 5+ years in content writing, copywriting, or editorial roles, with a strong portfolio of long-form and multi-channel work
- • Native-level written English with the ability to simplify technical jargon without losing its authority
- • A disciplined approach to claims, accuracy, and creating "review-ready" content for a regulated space
- • Experience using AI tools for research and efficiency, alongside an understanding of SEO/AEO (Answer Engine Optimisation)
🏖️ Benefits
- • Impactful work that helps patients gain access to potentially lifesaving treatments
- • Competitive salary, annual performance bonus, and an Employee Stock Option Plan
- • Attractive pension plan, full premium covered by myTomorrows
- • Hybrid working model
- • Unlimited access to professional guidance by certified psychologists via OpenUp
- • Healthy lunch at the thriving Amsterdam office
Skills & Technologies
Go
Senior
Hybrid
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.
Get more remote jobs like this
Subscribe to the weekly newsletter for similar remote roles and curated hiring updates.
Newsletter
Weekly remote jobs and featured talent.
No spam. Only curated remote roles and product updates. You can unsubscribe anytime.
Similar Opportunities
Expired
Brafton Inc.
South Africa remote
Full-time
Expired May 28, 2026
Remote
Degree Required
2 months ago