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The Associate Director of Biosample Operations will manage project activities related to biomarker strategies within clinical programs, ensuring continuity and integrity across projects. Responsibilities include overseeing biosample collection, coordinating assay development, and managing vendor operations. This role supports clinical operations with a focus on ensuring compliance and efficient biomarker sample management.

The Director of Pharmacometrics at Vir Biotechnology is responsible for leading the pharmacometrics strategy for drug development, collaborating with the Clinical Pharmacologist on pharmacometric activities, conducting modeling and simulations, and mentoring junior staff. The role involves applying quantitative modeling techniques to support clinical studies and regulatory submissions.

In this role, the Senior Director of Regulatory CMC is responsible for creating and executing regulatory strategies for clinical development and commercialization. This includes managing interactions with health authorities, ensuring compliance with regulatory requirements, and leading regulatory submissions. The ideal candidate will collaborate closely with Technical Operations and contribute to fostering a culture of high performance and continuous improvement.