Teams at Vir Biotechnology

Lead structuring, negotiation, and execution of complex biopharma partnering transactions for oncology assets. Drive deal strategy, financial terms, contract negotiation, diligence coordination, and cross-functional stakeholder alignment from term sheet to closing and post-signing governance.

Lead clinical pharmacology and pharmacometrics strategy across drug development stages. Design and execute PK/PD, PopPK, and exposure-response modeling; support study design, dataset preparation, regulatory documents, and cross-functional teams to inform dose selection from FIH through market authorization.

Lead and produce high-quality regulatory submission documents (protocols, IBs, CSRs, Module 2/5 summaries, labeling, briefing packages) for FDA/EMA. Ensure compliance with ICH/GxP, manage writing projects and timelines, collaborate with cross-functional teams, and define SOPs and best practices.