Jobs at Vir Biotechnology

Leads clinical pharmacology and translational PK/PD strategy and operations across preclinical and clinical drug development programs. Provides technical expertise on cross-functional teams, develops modeling and simulation approaches for dose selection, contributes to regulatory submissions, manages external collaborations and budgets, and builds and leads the clinical pharmacology team. The role supports infectious disease and oncology programs from pre-IND through market authorization.

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.

Provides comprehensive administrative support to executives, including complex calendar and meeting coordination, confidential information management, domestic and international travel arrangements, expense reporting, briefing materials, follow-up communications, special projects, and daily problem-solving. The role is fully onsite in San Francisco five days per week and requires discretion, organization, professionalism, and experience in the biotechnology or pharmaceutical industry.

Leads data engineering, cloud architecture, scientific software, and AI-enabled research platforms. Builds LLM, RAG, knowledge-search, and agentic workflows; integrates scientific systems; develops bioinformatics, genomics, clinical, and machine-learning data pipelines; and strengthens data quality, governance, lineage, security, observability, and reliability. Provides technical leadership across architecture, roadmaps, engineering practices, mentoring, and cross-functional collaboration.

Lead nonclinical toxicology strategy across infectious disease and oncology programs. Oversee GLP/non-GLP safety studies, design and interpret toxicology reports, support regulatory submissions (IND/BLA/CTAs/IMPDs), advise cross-functional teams, and drive safety risk assessment and lifecycle management.

The Senior Manager, Quality Control oversees QC strategy execution, ensuring timely delivery of testing activities and regulatory compliance across programs and testing partners.

Lead development, validation, and implementation of bioanalytical methods (PK, PD, ADA) for biologics; manage and mentor a bioanalytical team; oversee method transfers and CRO partnerships; support regulatory filings, audits, and cross-functional project planning to meet study objectives and compliance requirements.

Lead drafting, review and negotiation of clinical trial/site and vendor agreements for global multi-site studies. Manage end-to-end CTA processes and strategy, update templates and playbooks for country compliance, partner with Clinical Operations and Legal on risk and delivery, and co-manage external site contract/vendor service providers and governance.

Lead project management for partnered and internal research programs across discovery to early clinical development. Create integrated plans, track milestones and risks, facilitate cross-functional meetings, support governance and portfolio reviews, coordinate transitions to development, and drive research operations and strategic initiatives to improve governance, resource planning, and operational excellence.

Serve as a strategic, hands-on HR Business Partner for assigned client groups, advising leaders on workforce planning, organizational design, talent management, change management, performance, and employee experience. Coach managers, partner with HR centers of excellence, use people data to inform decisions, support HR program implementation, and enable organizational scaling and leader capability in an oncology-focused biotech environment.

Lead global, complex oncology clinical trials including vendor/CRO management, protocol and study document development, feasibility/start-up, maintenance and closeout. Manage study timelines, budgets, monitoring oversight, team members, and cross-functional stakeholder engagement while ensuring regulatory and GCP compliance.

Lead competitive intelligence for early-stage oncology programs by gathering and synthesizing external scientific and commercial insights (including LLM/agentic AI), maintaining competitor profiles, briefing senior leadership and cross-functional teams, and covering major conferences to inform clinical, program, and corporate decisions.