Vir Biotechnology

The Vice President will serve as the senior transaction lead for strategic partnering, responsible for structuring and negotiating complex oncology-focused deals. This role involves driving the full deal lifecycle while collaborating with internal teams to maximize the value of clinical and preclinical assets.

The Associate Director will represent clinical pharmacology on cross-functional teams to design, execute, and interpret clinical pharmacology data. They will apply quantitative modeling approaches like PK/PD and PopPK to guide dose selection and support regulatory submissions.

The role involves crafting clear, compliant regulatory documents for global health authorities such as the FDA and EMA. The writer will collaborate with cross-functional teams to manage timelines and ensure accurate scientific messaging across clinical programs.

The role involves crafting clear, accurate, and compliant regulatory documents for global health authorities such as the FDA and EMA. The writer will manage projects from planning to submission while collaborating with cross-functional teams to ensure content accuracy.

The role involves writing and editing regulatory documents such as protocols, IBs, and CSRs while ensuring accuracy and consistency. It also requires performing independent QC reviews and collaborating with cross-functional stakeholders to prepare global regulatory submissions.