Global Medical Director, Evidence Generation Lead

Global Medical Director, Evidence Generation Lead

About 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.

• Manage and lead partnerships and collaborative research projects with external stakeholders to advance disease and therapy data objectives.
• Drive the integration and validation of novel endpoints, including digital measures, to enhance personalized outcomes research.
• Accountable for strategic input into designing and execution of claims‑based analyses, observational studies, and real‑world evidence (RWE) studies.
• Lead and support Integrated Evidence Generation Planning (IEGP) forums, ensuring cross‑functional alignment and excellence in execution.
• Direct the design and analysis of phase 4 Company‑Sponsored Clinical Trials and secondary data analysis from real‑world data.
• Lead the collaboration with the R&D 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.
• Partner with the scientific communication lead to craft narratives and interpret data analytics for impactful storytelling.
• Ensure seamless collaboration with regional and affiliate medical teams to align global medical strategies with regional activities.
• Actively contribute to advancing best practices in evidence generation and medical research methodologies.
• Travel as needed to foster partnerships, collaborations, and project execution.

You 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.

• Advanced degree in the life sciences (MD, Neurologist, PhD, Pharm
  
  D, MPH, or equivalent).
• Minimum 10+ years of experience in the pharmaceutical industry, CRO/consulting firms, or academic institutions.
• Proven expertise in RWE activities, including a track record of successful scientific publications in peer‑reviewed journals.
• Strong knowledge of neurology, rare diseases, and clinical trials.
• Demonstrated ability to operate effectively in a highly matrixed organization.
• Exceptional interpersonal, influencing, and project‑management skills.
• Excellent written and oral communication, leadership, and presentation abilities.
• Experience collaborating with regional and affiliate medical teams to align activities with global medical strategy.
• Relevant experience in Medical Affairs or research and development.
• Ability to travel 30% as required.

• Expertise in registry studies, HEOR databases, and data analytics, including post‑hoc analyses.
• Familiarity with integrating digital and novel endpoints into research methodologies.
• Global experience in developing patient‑centric solutions for generating Real‑World Evidence (RWE).

Management

All 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.