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The Business Development Counsel will lead legal support for licensing and collaborations, oversee outside counsel, and ensure compliance with laws relevant to strategic alliances in biotechnology.

The Director leads data-driven strategies in biopharmaceutical manufacturing, overseeing intelligence and analytics to enhance decision-making and operational priorities. Responsibilities include developing insights, managing analytics products, and leading cross-functional alignment.

The PO&T Risk Management Lead oversees risk management processes within Biogen, collaborating with leadership to assess and mitigate organizational risks and enhance business continuity efforts.

Lead US HCP marketing for General Nephrology launches (AMR, MVI) and IgAN expansion. Develop branded and unbranded HCP strategies, omnichannel campaigns, and 3-year brand roadmaps. Manage team, budgets, agencies, cross-functional partners, and market/competitive insights to drive HCP education, activation and referrals.

The Executive Medical Director leads early clinical development in immunology, oversees drug asset programs, and collaborates across functions for successful trials and strategic initiatives.

The Sr Tech II calibrates and repairs instrumentation, supports engineering activities, and modifies procedures to enhance operations in manufacturing and laboratories.

The Principal Clinical Data Reviewer/Scientist leads clinical data review activities, ensuring data quality and integrity, and collaborates with cross-functional teams to support clinical trial execution and risk management.

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

Manufacturing Associates operate equipment, execute cGMP processes, document activities, conduct sampling, maintain safety, and participate in team training at a drug substance facility.

The Principal Scientist will develop biomarker strategies for clinical studies, oversee data interpretation, collaborate with cross-functional teams, and contribute to regulatory submissions in the field of solid organ transplant research.