Evidence Strategy

Make your mark for patientsTo strengthen our Rare & Epilepsy organization, we are looking for an Evidence Strategy & Development Manager Rare & Neurology (m/f/d), to be based in Monheim, Germany.About the roleAs Evidence Strategy & Development Manager Rare & Neurology (m/f/d) , you will shape and execute a comprehensive evidence generation strategy for Rare & Neurology in Germany. You will lead Real-World Evidence and Post-Approval research, provide strategic input into global pipeline programs considering German HTA/AMNOG requirements, and ensure local medical needs are integrated into global studies. The role includes driving cross-functional evidence workstreams, leading publication strategy, and fostering partnerships with academic institutions while promoting innovative, digital approaches. Your mission: scientific excellence, compliance, and creating value for patients.Who you’ll work withYou will collaborate closely with Medical Affairs, Market Access, Global Clinical Development, as well as European and global Medical and Development teams. Additionally, you will build strategic partnerships with academic institutions, networks, and external experts. This role reports directly to the Head of Medical Rare & Neurology Germany.What you’ll doDevelop and implement a national evidence generation strategy for Rare & NeurologyIdentify critical data gaps for our assetsLead Real-World Evidence programs and Post-Approval studies (NIS, IIS, registries)Provide strategic medical input into global development and pipeline programs to ensure German clinical practice and HTA/AMNOG requirements are reflectedPlan and execute national publication strategiesBuild and maintain partnerships with research institutions and professional societiesDrive innovative approaches such as digital data sources and analyticsRepresent the affiliate in European and global Evidence Generation & Pipeline networks to drive alignment and share best practicesFor this role we’re looking for the following education, experience and skills:Education: M.D. preferred, Pharm.D., or natural sciencesExperience: Several years in Medical Affairs, clinical development, or R&D, ideally in neurology and/or rare diseasesExpertise: Real-World Evidence, non-interventional research, publication planning, dossier writing and scientific contribution to G-BA negotiationsKnowledge: German regulatory requirements, AMNOG and HTA processes, ICH-GCP guidelines, local laws, and regulatory requirementsSkills:Strategic thinking and scientific leadershipStrong communication skills in German and EnglishAbility to lead projects and collaborate cross-functionallyInnovation mindset and digital affinityIntegrity and compliance awarenessInterested?Apply now and join our Patient Impact team Together, we shape the future of evidence-based medicine and improve patient care in Germany.Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you