Ph3Global Medical Director, Evidence Generation Lead /h3pAbout This Role: As the Global Medical Director, Evidence Generation Lead, you will play a pivotal role in advancing data generation initiatives for the Dravet Syndrome therapeutic area. This position resides within the Global Medical Dravet Syndrome team and is central to driving collaboration, innovation, and excellence in research. You will lead partnerships and collaborative efforts with external stakeholders to generate disease and therapy‑specific data, integrate novel endpoints like digital measures, and empower patients to produce Real‑World Evidence (RWE). Your expertise will be instrumental in ensuring alignment across teams and executing RWE studies, e.g., setting up and overseeing patient registries for natural history data and zorevunersen RWE data collection, data analysis, and collaborative research with identified centers of excellence. By leveraging your deep knowledge of neurology, rare diseases, and evidence generation, you will directly contribute to shaping the future of personalized outcomes research and medical advancements. This is a unique opportunity to make a meaningful impact in a highly matrixed and dynamic environment. /ph3What You’ll Do /h3ulliManage and lead partnerships and collaborative research projects with external stakeholders to advance disease and therapy data objectives. /liliDrive the integration and validation of novel endpoints, including digital measures, to enhance personalized outcomes research. /liliAccountable for strategic input into designing and execution of claims‑based analyses, observational studies, and real‑world evidence (RWE) studies. /liliLead and support Integrated Evidence Generation Planning (IEGP) forums, ensuring cross‑functional alignment and excellence in execution. /liliDirect the design and analysis of phase 4 Company‑Sponsored Clinical Trials and secondary data analysis from real‑world data. /liliLead the collaboration with the RD team and Global Value Access team on data analytics initiatives (e.g., outcomes on subgroups, correlation of endpoints), including registry studies, HEOR databases, and post‑hoc analyses. /liliPartner with the scientific communication lead to craft narratives and interpret data analytics for impactful storytelling. /liliEnsure seamless collaboration with regional and affiliate medical teams to align global medical strategies with regional activities. /liliActively contribute to advancing best practices in evidence generation and medical research methodologies. /liliTravel as needed to foster partnerships, collaborations, and project execution. /li /ulh3Who You Are /h3pYou are a visionary leader with a passion for advancing medical research and evidence generation in neurology and rare diseases. You thrive in a collaborative environment and excel at building strong partnerships with diverse stakeholders. Your analytical mindset enables you to approach challenges with precision, while your interpersonal skills foster alignment and inspire teams toward shared goals. You are motivated by the opportunity to empower patients, innovate research methodologies, and drive impactful outcomes that make a difference in the lives of those affected by Dravet Syndrome. /ph3Required Skills /h3ulliAdvanced degree in the life sciences (MD, Neurologist, PhD, PharmD, MPH, or equivalent). /liliMinimum 10+ years of experience in the pharmaceutical industry, CRO/consulting firms, or academic institutions. /liliProven expertise in RWE activities, including a track record of successful scientific publications in peer‑reviewed journals. /liliStrong knowledge of neurology, rare diseases, and clinical trials. /liliDemonstrated ability to operate effectively in a highly matrixed organization. /liliExceptional interpersonal, influencing, and project‑management skills. /liliExcellent written and oral communication, leadership, and presentation abilities. /liliExperience collaborating with regional and affiliate medical teams to align activities with global medical strategy. /liliRelevant experience in Medical Affairs or research and development. /liliAbility to travel 30% as required. /li /ulh3Preferred Skills /h3ulliExpertise in registry studies, HEOR databases, and data analytics, including post‑hoc analyses. /liliFamiliarity with integrating digital and novel endpoints into research methodologies. /liliGlobal experience in developing patient‑centric solutions for generating Real‑World Evidence (RWE). /li /ulh3Job Level /h3pManagement /ph3Equal Employment Opportunity /h3pAll qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information, or any other basis protected by federal, state or local law. Biogen is an E‑Verify Employer in the United States. /p /p #J-18808-Ljbffr