Jobs at Biogen

The National Director will develop and execute a US thought-leadership engagement plan for Nephrology, collaborating closely with several teams to drive strategic priorities and manage resources.

As Senior Manager of IT Commercial Data Management, you will lead data initiatives, manage product ownership, and develop data governance strategies in collaboration with stakeholders, ensuring high data quality and analytics capabilities.

Lead quality oversight for clinical studies by ensuring GCP compliance, managing risk assessments, investigations, CAPAs, and inspection readiness. Partner with internal and external stakeholders, support audit planning, approve controlled documents, and drive process improvements across RD&M.

Own and administer Biogen's Small Business Subcontracting Plan (SBSP), ensure federal compliance and audit readiness, maintain supplier diversity data, integrate ESG/diversity into sourcing decisions, support sourcing teams, perform spend analytics, produce government and ESG reports, and represent the company in supplier diversity networks.

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

The Associate Scientific Director will lead pharmacometrics analyses, contribute to drug development strategies, mentor colleagues, and support decision-making through advanced quantitative modeling.

Lead clinical development activities for early-phase neuroimmunology programs (I-II). Design protocols, provide medical monitoring, oversee study execution, collaborate cross-functionally and with CROs, support regulatory interactions, interpret data, and incorporate patient-centered approaches to advance immunology drug candidates.

Oversee clinical pharmacology plans for drug candidates, lead studies, analyze pharmacokinetic data, and engage with health authorities to guide drug development strategies.

Lead the Informed Consent Management (ICM) function supporting study start-up and maintenance for global clinical trials. Triage ICF requests, advise on IRB/EC changes, author Global Master ICFs, oversee CRO consent activities, monitor compliance and KPIs, produce metrics, and drive process improvements and SOP/Work Instruction maintenance to ensure timely, high-quality informed consent documentation.