
Job Overview
Location
US, Remote
Job Type
Full-time
Category
Product Marketing Manager
Date Posted
May 21, 2026
Full Job Description
đź“‹ Description
- • Own the end-to-end product narrative for myTomorrows’ offerings in clinical trials and Expanded Access Programs, clearly differentiating the platform from legacy databases and lead-gen tools by articulating unique value to physicians, trial sites, and BioPharma sponsors.
- • Translate complex product capabilities into clear, actionable messaging that aligns with real-world workflows of healthcare professionals, reducing friction and increasing adoption rates across global clinical research environments.
- • Act as the primary voice of the market by synthesizing feedback from trial sites, physicians, patient advocacy groups, and BioPharma clients to inform product roadmap priorities and feature development.
- • Develop and deliver product-native enablement assets—including narratives, workflow diagrams, value frameworks, and use-case guides—that empower Commercial, Medical, and Growth teams to confidently communicate product benefits to stakeholders.
- • Lead end-to-end product launch readiness for new features, ensuring cross-functional alignment on messaging, positioning, and use-case clarity across internal teams prior to public release.
- • Build and maintain a fast-paced feedback loop between end users and the Product team, replacing internal assumptions with real-world clinical insights to drive product improvements and user-centric innovation.
- • Drive measurable improvements in referral-to-enrollment conversion by refining localized messaging that reflects regional regulatory, operational, and protocol constraints in the global drug development ecosystem.
- • Collaborate closely with Product, Commercial, and Medical leadership to align go-to-market strategies with customer needs, ensuring product positioning reflects the realities of rare disease pathways and trial site operations.
- • Create scalable, jargon-free communication frameworks that enable teams to articulate the platform’s value in under 60 seconds, ensuring consistency and clarity in all external and internal stakeholder interactions.
- • Support global expansion by adapting messaging and workflows to regional healthcare systems and regulatory environments while maintaining a unified brand and product narrative across 134 countries.
- • Ensure all marketing materials and internal tools reflect the ethical and compassionate mission of enabling earlier access to potentially lifesaving therapies for patients with unmet medical needs.
- • Maintain deep understanding of the regulatory landscape surrounding Expanded Access Programs (EAPs), clinical trial protocols, and real-world data collection standards to ensure all messaging is compliant and credible.
- • Proactively identify gaps in stakeholder understanding of product functionality and design targeted educational content to bridge those gaps and accelerate user adoption.
- • Work within a flat, international organizational structure that encourages autonomy, creativity, and accountability, contributing to a culture that values diversity and innovation in health tech.
🎯 Requirements
- • Deep, proven experience within the BioPharma, Clinical Trials, or Expanded Access (EAP) ecosystem, including understanding of regulatory, operational, and protocol-driven constraints.
- • 4–6 years of experience in Product Marketing or Product Strategy within HealthTech, digital health, or biopharma.
- • Exceptional structured thinking with the ability to map complex product capabilities to real-world user outcomes and translate them into compelling narratives.
- • Relentless ownership and follow-through, taking accountability for outcomes—not just outputs.
- • Comfortable navigating 0-to-1 environments and collaborating closely with Product, Commercial, and Medical stakeholders.
- • Deep understanding of the distinct workflows and pain points of trial sites, rare disease ecosystems, and pharma teams.
🏖️ Benefits
- • Impactful work that helps patients gain access to potentially lifesaving treatments.
- • Competitive salary, annual performance bonus, and an Employee Stock Option Plan.
- • 401(k) retirement plan automatically enrolled for all US employees.
- • 25 days of paid time off per year for full-time employees.
- • 5 days of fully paid sick leave per year.
- • Learning and development budget alongside internal knowledge sharing sessions.
- • International work environment, scale-up energy, and a flat organizational structure encouraging creativity and accountability.
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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