Global Medical Lead Early Assets

Professional | Permanent | Full-time | HybridAre you an entrepreneurial thinker? Do you want to join a dynamic team with a strong sense of purpose that thrives on finding new ways to tackle challenges? Then our Commercial, Marketing & Sales team is the right place for you: whether you’re passionate about Marketing, Medical Affairs, Market Access, Commercial Excellence or Sales. We analyse the market to find out exactly what patients need, and then we provide pain treatments that improve their lives – while creating value for Grünenthal. We strive to make progress towards our vision of a world free of pain – every single day, one patient at a time. We’d love you to help us make a powerful impact on the lives of people living with pain around the globe.What The Job Looks LikeEach day you’ll enjoy a variety of challenges, such as:Responsible for establishing the KEE, patient Organization and Scientific Societies network in DMDProvides PAG engagement plan and engages with PAGs, supports with KEE engagement plan and engages with KEEs including the organization of patient and KEE advisory boardsWorks in close collaboration with the Global Medical Lead Early Assets, R&D project lead, and the commercial lead for early products to define the TPP and product hypothesis that will drive development effortsSimilarly, works with the early stage diligence team to crystalize the potential value of a R&D –stage product by defining the TPP, product hypothesis to enable positioning in most appropriate area of relevant medical needGuides & leads scientific discussions, incl. further study program and LCM initiatives aimed at enhancing outcomes e.g. identify patient profiles with highest benefit from intervention/treatment.Develops scientific/medical story flow and scientific narratives, including scientific messaging accuracy and dissemination across stakeholders in line with patient journey, unmet needsUnderstands the competitive landscape and provides regular reports and training on the matter across the businessAligns evidence generation planning with regulatory, clinical, and commercial goals. identifies evidence gaps for regulators, payers, prescribers, and patients.Outlines clinical trials, real-world studies, HEOR, biomarker research, etc. Connects insights across R&D, Medical Affairs, and Commercial functionsWhat You’ll Bring To The TableTo make the most of this role and truly thrive, you should have:Experience in interacting with PAG in rare diseases. Experience with DMD PAGs as a plusPassionate about connecting with External Stakeholders and building strong network with KEE, Patient Advocacy Groups and relevant stakeholders.Excellent understanding of clinical practice, guidelines and existing standards in rare diseases / DMDExperience in early products evaluation and drug developmentComprehensive knowledge of applicable compliance, legal & regulatory requirementsThorough medical and scientific acumen Passionate about medical affairs and creating value for patients and seeking insights into real clinical practicePreferably knowledgeable about biological pathways of DMD disease and available therapiesPreferably knowledge in building Integrated Evidence Plans and working closely with US ______________________________________ "Great o pportunity to participate in building the capabilities in rare diseases "Ana Cerdeira , the Hiring Manager