Jobs at Biogen

Oversee external CDMO manufacturing operations for pharmaceutical and biologic products, including assembly, labeling, packaging, technology transfers, change controls, deviations, process control, and continuous process verification. Lead supplier governance, performance reviews, corrective actions, business optimization, and cross-functional teams while ensuring regulatory compliance, quality, efficiency, and cost effectiveness.

Provides strategic employment-law counsel to Global Human Resources and business leaders across the employee lifecycle. Advises on workplace investigations, disputes, litigation, compliance, governance, cross-border workforce matters, policies, audits, and risk mitigation. Manages outside counsel and legal budgets, monitors regulatory developments, delivers training, and supports organizational transformations across Biogen’s global workforce.

Design, execute, analyze, and interpret experiments in neuromuscular disease research using iPSC-derived and primary human muscle and cardiac models, rodent phenotyping, molecular/biochemical assays, and statistical analysis. Collaborate across teams and present findings to advance therapeutic programs.

Leads enterprise insights and analytics for Biogen’s US Commercial organization. Establishes and manages the LEQEMBI Control Tower, integrates cross-functional brand and market insights, operationalizes insight-to-action processes, monitors performance, and translates analytics into strategic decisions. The role coordinates stakeholders, facilitates collaboration forums, recommends resource allocation, and presents findings to executive and cross-functional audiences within a pharmaceutical environment.

Leads strategy execution, operating cadence, strategic planning, cross-functional initiatives, executive communications, business reviews, and organizational communications for Biogen’s IMNDU development organization. Translates priorities into actionable workstreams, tracks goals and performance, facilitates governance forums, supports senior leadership decisions, and aligns communications across a global biopharma enterprise.

Leads the architecture, implementation, and governance of enterprise IAM solutions using SailPoint and ServiceNow. Designs access lifecycle, provisioning, certifications, role management, application integrations, and segregation-of-duties controls. Provides technical leadership, conducts architecture reviews, manages implementation roadmaps, supports audits, and ensures GxP and SOX compliance. Partners with cybersecurity, infrastructure, applications, quality, business teams, and senior stakeholders while mentoring IAM personnel.

Leads strategy execution, operating cadence, strategic planning, cross-functional initiatives, portfolio prioritization, and executive communications for Biogen’s SPARQ organization. Translates priorities into workstreams, timelines, ownership, metrics, and progress tracking; facilitates leadership forums and business reviews; develops executive narratives and communications; and partners with R&D and Corporate Communications to ensure aligned messaging and employee engagement.

Leads launch excellence and change management for Biogen North America’s commercial enablement initiatives. Translates therapeutic-area priorities into coordinated plans, aligns field readiness, CRM, decision sciences, marketing operations, omnichannel, patient services, and digital operations, and manages milestones, dependencies, risks, and issue resolution. Drives adoption through communications, training, governance, playbooks, and operating rhythms. Requires strong executive communication, project management, cross-functional influence, and 8+ years in pharma, biotech, or life sciences consulting, including U.S. product launch experience.

Leads Biogen’s enterprise data stewardship and AI-ready data engineering organization supporting clinical development. Owns data governance, architecture, standards, SDTM, transparency, controlled data sharing, imaging data, reusable data products, submission-ready pipelines, and machine-learning enablement. Defines strategy, operating models, decision rights, roadmaps, and investments while partnering across clinical, regulatory, legal, privacy, technology, and scientific functions. Builds and leads an approximately 24-person organization and drives compliant, scalable, interoperable, and responsible AI-ready data capabilities.

Leads development, deployment, and optimization of machine learning, AI, and predictive analytics solutions for U.S. Commercial operations. Builds models using claims, EHR, specialty pharmacy, and commercial data to analyze patient populations, provider behavior, treatment patterns, adherence, and engagement. Partners with Commercial, Medical Affairs, and analytics teams to translate insights into business strategies, while managing vendors, supporting model governance, and communicating findings to leadership.

Leads organizational change and adoption for AI initiatives, Planisware enhancements, workflow automation, and reporting modernization across drug development. Develops stakeholder engagement, communications, training, readiness, and reinforcement strategies; builds change champion networks; tracks adoption and value-realization metrics; supports responsible AI use; and coordinates user acceptance testing, go-live readiness, and post-implementation monitoring.

Provides executive administrative support to the Head of US Specialty Immunology through complex calendar and meeting management, presentation preparation, travel coordination, expense reporting, purchasing and invoice support, onboarding, communications, and team culture activities. The role requires discretion, sound judgment, strong organization, proactive problem-solving, and proficiency with Microsoft Office 365 tools while collaborating across leadership and administrative teams.

Leads clinical genetics and pharmacogenomics strategy across Phase I–III programs. Responsibilities include designing genetic testing strategies, advising on clinical trial protocols, interpreting genomic findings, managing testing vendors, addressing regulatory and ethical considerations, and translating clinical genetics insights into development, patient stratification, and reverse translational research decisions.

Manages and executes ITGC testing for SOX 404 compliance, including planning, walkthroughs, design and operating effectiveness testing. Reviews audit evidence and documentation, identifies control deficiencies, supports remediation, and coordinates with IT, risk management, SOX PMO, internal audit, and external auditors. Oversees junior staff, ensures testing quality and timelines, and supports IT audits, risk assessments, and internal audit initiatives outside peak SOX periods.

Leads the design, implementation, enhancement, integration, testing, and support of Veeva Vault RIM. Translates business requirements into functional specifications, manages application roadmaps, supports GxP compliance, mentors technical resources, oversees vendors, and drives system optimization. The role also handles data activities for mergers and divestitures, investigates emerging technologies, and partners with business and IT stakeholders to deliver reliable regulatory information management services.

Leads Biogen’s global clinical trial start-up and study activation strategy from protocol finalization through site initiation. Oversees activation teams, processes, systems, vendors, contracting, budgeting, EU-CTR strategy, compliance, and cross-functional delivery. Drives technology-enabled process improvement, performance visibility, talent development, and inspection-ready execution across regions and therapeutic areas.

Provide high-level administrative support to an Executive Officer: manage complex calendars, coordinate leadership meetings and governance, draft executive communications, triage email, maintain org documents and SharePoint, arrange domestic and international travel, process expenses, provide in-person support for international strategic sessions, and collaborate with PO&T teams to drive initiatives and cross-organizational alignment.

Senior immunology drug development leader serving as a strategic advisor and delegate to the unit head. Leads research-to-development transitions, early clinical development strategy, portfolio decisions, external innovation, business development, and venture investment assessments. Integrates scientific, clinical, regulatory, commercial, and strategic perspectives while aligning cross-functional teams, evaluating opportunities, guiding governance decisions, mentoring colleagues, and advancing programs from preclinical development through proof of concept.

Leads pharmacovigilance activities for assigned products, including signal detection and management, literature reviews, safety inquiries, and aggregate reports such as PSURs, DSURs, REMS, and RMPs. Collaborates on clinical trial safety activities, regulatory responses, data analysis, and cross-functional product information sharing. Serves as a subject matter expert on global safety regulations and may hire, train, and mentor product-specific staff.

Leads global commercial supply operations for a biotech/pharmaceutical organization, including third-party packaging, labeling, and logistics partners. Oversees supplier governance, 3PL performance, inventory control, launch readiness, contracts, compliance, serialization, DSCSA requirements, risk mitigation, and continuous improvement. Manages teams and cross-functional initiatives while ensuring supply continuity, quality, service, and cost objectives. Requires extensive pharmaceutical supply chain leadership experience and occasional supplier travel.