Vir Biotechnology
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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.
The Senior Director of Corporate Communications at Vir Biotechnology will develop and execute communication strategies that convey the company's value and support business objectives. Responsibilities include crafting PR materials, building media relationships, managing internal and external communications, and enhancing Vir's visibility in the industry.
This role involves overseeing the operations of the Research Department, managing research project portfolios, budget management, fostering stakeholder engagement, and developing a high-performing team. The Director will implement best practices for operational excellence and contribute to strategic planning and research governance.
As the Director of Biostatistics at Vir Biotechnology, you will provide technical leadership in clinical development programs, acting as a statistical expert and leading drug development projects. Responsibilities include optimizing trial designs, executing statistical deliverables, conducting simulations, and overseeing clinical protocol development, while ensuring compliance with regulatory standards.