Biogen Global Associate Medical Director – SMA Life Cycle Management in Cambridge, Massachusetts
About This Role: * The *Global Associate Medical Director - Spinal Muscular Atrophy (SMA) Life Cycle Management (LCM) is a member of the Global Medical SMA team and will report to the Sr. Global Medical Director Lead - SMA. You will be responsible for supporting the life cycle management of marketed products in SMA and late phase pipeline assets. You will work closely with the evidence generation, biostatistics, clinical development, and clinical operations program teams to plan and execute global medical affairs studies. What You'll Do: * Support the development of the SMA global medical affairs strategy and tactics * Work closely with the evidence generation team to develop the integrated evidence generation plan for SMA aligned with the global medical strategy * Review external research proposals and ensures alignment with global medical strategy * Develop study designs (non-registration phase IIIb/IV, registries, outcomes research) and works closely with study teams to execute study protocols and address study related questions * Manage on-going studies in close collaboration with relevant functions * Lead pre-launch, launch and post-launch medical activities and represents medical in global cross-functional teams *Who You Are: * You have experience with study design/clinical trial design and protocol development. You might be in clinical development and are looking to transition into a global medical affairs role or are a medical doctor/nurse/clinical research lead that wants to join medical affairs. #LI-JR1 *Required Skills: * * MD, PhD, PharmD or other advanced degree in the life sciences required * Minimum 3+ years of pharmaceutical industry experience is required, preferably in SMA, neuromuscular diseases, or neurology/neuroscience * Experience in clinical research in a clinical scientist/clinical development/clinical trial manager role, or significant relevant experience in clinical trials * Demonstrated experience reviewing clinical data and statistical outputs * Demonstrated ability to effectively engage with steering committees and investigators * Ability to critically analyze and synthesize complex scientific information All your information will be kept confidential according to EEO guidelines.