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The Associate Scientific Director will lead clinical pharmacology efforts, providing expertise throughout drug development, conducting analyses, and collaborating with teams on project goals.

Lead biomarker operations across clinical development, ensuring high-quality data delivery, team management, cross-functional collaboration, and compliance with standards.

As a Clinical Development Lead at Biogen, you will oversee the development of therapies for rare autoimmune nephrology diseases, guiding clinical trials, collaborating with scientists and stakeholders, and ensuring compliance with regulatory standards.

The Sr. Manager, Clinical Trial Lead oversees clinical studies by developing operational strategies, collaborating with cross-functional teams, and managing CRO performance to ensure successful trial execution within budget and timelines.

The Senior Manager, Global Labeling oversees the development and compliance of product labeling, ensuring regulatory standards are met and leading cross-functional collaboration for product success.

The Associate Director will provide regulatory strategic advice for U.S. communications, ensuring compliance with FDA regulations while collaborating with cross-functional teams to support materials for healthcare providers, payors, and patients.

The Associate Scientific Director, Pharmacometrics will provide expertise in pharmacometrics for drug development, collaborating with teams on modeling, simulation, and quantitative analysis to inform decision-making and regulatory documentation.

The Clinical Trial Management PV Lead ensures operational excellence and compliance in safety processes and data quality within clinical studies, leading initiatives in pharmacovigilance and cross-functional collaborations.