Jobs at Biogen

Process regular and off-cycle US payroll, calculate payroll inputs, ensure tax and regulatory compliance, audit records, resolve employee and stakeholder requests, maintain documentation, improve payroll systems and processes, and support Canada payroll processing. The role also provides backup support, participates in payroll projects, and collaborates with multiple departments and stakeholders while working Eastern Standard Time hours.

Leads the insourced FSP operating model for country and site clinical trial operations. Manages 20–25 FSP staff, resource forecasting, assignments, budgets, training, onboarding, vendor governance, performance metrics, and quality expectations. Partners with clinical operations, study teams, Medical, Quality, and regional stakeholders to improve trial execution, scalability, efficiency, and cost effectiveness. Oversees processes, risk management, stakeholder alignment, and continuous improvement across global clinical development activities.

Provides strategic leadership for Clinical Pharmacology across transplant development programs, including dose selection, exposure-response and population PK analyses, regulatory submissions, BLA/NDA support, health authority interactions, labeling, lifecycle management, and filing readiness. The role leads cross-functional strategy, mitigates regulatory risks, mentors colleagues, and represents Clinical Pharmacology in governance and program teams.

Leads Country and Site Operations teams supporting global clinical trials. Responsibilities include line management, coaching, workforce and workload planning, operational oversight, sponsor and CRO/FSP partnership, site and investigator engagement, escalation management, inspection readiness, and cross-functional collaboration. The role also drives capability development, process improvement, portfolio risk management, and country/site strategy across multiple studies and therapeutic areas.

Leads end-to-end clinical trial operations, including study strategy, protocol development, CRO oversight, risk mitigation, quality, timelines, budgets, and compliant execution. Chairs study management teams and coordinates cross-functional drug development activities across neurological and nephrology programs. Requires strong clinical operations leadership, GCP and ICH expertise, CRO management, project management, and scientific knowledge.

Supports early-phase immunology and neuroimmunology clinical development programs, including protocol design, trial execution, medical monitoring, data interpretation, regulatory interactions, safety planning, and clinical documentation. Partners with cross-functional R&D teams, CROs, investigators, and external stakeholders while providing therapeutic expertise and monitoring developments in autoimmune disease.

Leads enterprise architecture for Biogen’s Veeva ecosystem across Development, Quality, Regulatory, Safety, and Commercial functions. Translates business needs into scalable Veeva configurations and integrations, governs target-state architecture and platform standards, reviews solution designs, and oversees implementation and release planning. Mentors configuration teams, drives cross-vault consistency, manages architecture governance, aligns with Veeva product roadmaps, and advises IT leadership on platform strategy, investments, regulatory compliance, and business objectives.

Lead biostatistical efforts in clinical research, oversee analysis plans, mentor junior staff, and ensure statistical integrity. Key role in data analysis and regulatory submissions.

Support the Country and Site Lead by providing local operational and scientific expertise to inform clinical development strategy. Act as single point of contact for CROs, affiliates, and global teams; drive site engagement, monitor country performance (KPIs), support site selection, resolve investigator/site issues, and oversee sponsor oversight activities. Field-based role with heavy travel to enable trial delivery and quality.