Jobs 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.

Create, edit, and ensure compliance of regulatory submission documents (protocols, IBs, CSRs, Module 2/5 summaries) for global health authorities. Translate complex clinical data into clear text, coordinate cross-functional inputs, manage writing timelines, and advise teams on regulatory writing best practices to support IND/NDA/MAA and other submission activities.

Perform regulatory writing and editorial/QC for submission documents (protocols, IBs, CSRs, briefing packages, NDA/IND/MAA components). Verify accuracy and consistency versus source data, apply style guides and templates, proofread and copyedit, prepare eCTD/CTD submission materials, communicate QC findings, manage document workflows and timelines, and improve QC tools and SOPs.