Lead and execute the in-country regulatory strategy and serve as the senior interface with Indian Health Authorities for Biogen's portfolio. Manage product registrations, lifecycle changes, and compliance for rare and high unmet-need diseases in India.
Biogen
15 Remote Job Openings at Biogen
Director, Corporate Affairs, Global Product Communications Alzheimer’s Disease
Biogen
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Full Time
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4 days ago
Biogen
Lead the development and execution of integrated global product communications strategies for the Alzheimer's Disease franchise. Collaborate cross-functionally to craft science-driven narratives and manage news flow for approved and investigational medicines.
The Associate Director serves as a strategic partner to the Head of Sales, managing the operational cadence and business governance of the Neuropsychiatry sales organization. This role focuses on translating leadership priorities into measurable execution, driving organizational effectiveness, and coordinating cross-functional initiatives.
Associate Director, Access Management Service Delivery- Cyber Security
Biogen
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Full Time
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7 days ago
Biogen
Lead the delivery of global access management services, establishing policies, standards, and automation strategies to improve service efficiency. Manage the full lifecycle of digital identities and ensure compliance with regulatory requirements like SOX and GxP.
Lead and coach the Partnership Account Lead sales team to drive growth of the Biogen Canada portfolio across all therapeutic areas. Collaborate with cross-functional partners to implement national sales strategies and track key performance indicators.
Manage the Small Business Subcontracting Plan to ensure federal compliance and drive sustainable spending. Integrate diversity and ESG criteria into procurement processes and supplier selection decisions.
Contribute to the design and execution of early-phase clinical trials for immunology programs focusing on autoantibody-driven diseases. Partner with cross-functional teams to develop protocols, provide medical monitoring, and support regulatory interactions.
The ARM ensures patient access to therapies by managing reimbursement strategies and collaborating with neurology accounts and infusion providers. They act as a liaison to resolve complex billing and coverage issues while delivering educational programs to healthcare providers.
Drive strategic scientific engagement and provide medical support to key experts and patient advocacy groups to bolster pipeline development in Germany. Lead expert discussions, deliver complex scientific presentations, and collect medical insights to inform local strategy.
Lead the Medical Writing function for the West Coast Hub, overseeing the development of complex clinical and regulatory documentation for nephrology and immune-mediated disease portfolios. Manage a team of writers and external vendors while driving process improvements and cross-functional alignment within R&D.
Drive global clinical development strategies by providing local operational and scientific expertise in Canada. Manage relationships with investigators and oversee CRO activities to ensure patient safety, data integrity, and regulatory compliance.
The Medical Science Liaison acts as a scientific expert to engage with Key Medical Experts and healthcare professionals to improve clinical decision-making and patient outcomes. They are responsible for executing medical strategy, capturing clinical insights, and fostering long-term strategic relationships within their assigned territory.
The Associate Director will provide pharmacometrics expertise for high-priority clinical development programs, contributing to strategy and supporting quantitative decision-making through advanced modeling and simulation. This role involves executing advanced analyses like PK/PD modeling and communicating results to program teams to support data-driven decisions.
The Associate Scientific Director will provide strategic leadership in developing and executing clinical pharmacology plans for drug candidates, integrating knowledge to optimize dosage regimens and study designs throughout the drug development lifecycle. This role involves leading the execution of clinical pharmacology studies, conducting hands-on quantitative analysis, and serving as the subject matter expert in interactions with Health Authorities.
The Clinical Country Site Lead (CCSL) provides local operational and scientific expertise to support global clinical development strategy and ensures the delivery of local clinical trials. This role acts as a primary contact for CRO staff and global teams, focusing on quality, patient safety, and oversight of monitoring activities.
