Jobs at Vir Biotechnology

Leads oncology development programs as the cross-functional program executive and single point of accountability. Defines clinical and development strategy, integrated plans, milestones, evidence requirements, resourcing, budgets, and risk mitigation. Partners with executives, governance committees, regulatory authorities, investigators, and external stakeholders. Guides trial planning, biomarker and patient-selection strategies, indication prioritization, data interpretation, lifecycle planning, and value-inflection milestones. Coordinates clinical, regulatory, operational, safety, commercial, and technical functions while mentoring program leaders.

Supports oncology clinical studies from startup through reporting, including protocol and consent development, clinical data review, site-facing activities, study analyses, regulatory submissions, and clinical documentation. Partners with Clinical Operations, Medical Monitoring, Data Management, Biostatistics, and Regulatory teams to ensure high-quality study execution and interpretation of emerging data.

Provides strategic and operational leadership for global early-phase oncology clinical trials. Leads study teams, CROs, vendors, site and enrollment strategies, budgets, timelines, risk management, regulatory activities, inspection readiness, and sponsor oversight. Partners cross-functionally on clinical development and portfolio strategy, supports alliance programs, drives process improvements and SOP development, and mentors Clinical Operations staff.

Leads cross-functional CMC development programs from early development through regulatory filing and commercial lifecycle management. Responsibilities include integrated project planning, vendor and CMO coordination, risk mitigation, critical-path analysis, portfolio reporting, budgeting, resource forecasting, process improvement, and operational excellence across CMC functions.

Provides strategic leadership and governance for the company’s Quality Management System in a GxP environment. Oversees document control, training, audits, CAPA, investigations, change control, risk management, and quality metrics. Leads inspection readiness, regulatory inspections, audit management, remediation, quality assessments, and continuous improvement initiatives supporting clinical development, regulatory submissions, and commercialization readiness.

Supports quality oversight for pharmaceutical and biotechnology manufacturing, testing, packaging, and labeling activities at internal and external partners. Reviews deviations, CAPAs, change controls, investigations, SOPs, batch records, validation documents, and release materials. Assists with batch disposition, supplier quality management, audits, regulatory inspection readiness, quality agreements, issue escalation, and continuous improvement while ensuring cGMP and regulatory compliance.

Support clinical and commercial stability programs for biologics by coordinating external studies, reviewing and trending stability data, managing LIMS data and metadata, supporting investigations and protocol documentation, and preparing reports for internal teams and regulatory submissions. The role collaborates with Analytical Development, Quality, Regulatory, Supply Chain, CDMOs, CLOs, and other external partners.

Senior hands-on engineer responsible for hybrid infrastructure operations and IT security. Maintains Windows, macOS, Linux, cloud, networking, virtualization, identity, endpoint, and security environments; investigates incidents, vulnerabilities, and alerts; supports incident response, access management, audits, and compliance; and develops automation and documentation. The role requires troubleshooting across complex systems, improving security controls and operational processes, and collaborating with IT teams, stakeholders, vendors, and managed service providers. The position is temporary and requires working onsite in San Francisco four days per week.

Coordinates biospecimen transaction tracking, shipment records, sample returns, destruction documentation, database maintenance, and reporting. Develops manual or automated reporting plans using Excel, Smartsheet, or programming solutions; collaborates with laboratories and external partners to resolve discrepancies and maintain regulatory and organizational data standards.

Serves as a strategic HR partner to assigned business groups, advising leaders and managers on employee relations, performance management, workforce planning, talent management, organizational change, and employee engagement. Builds trusted relationships, supports manager capability, analyzes workforce data and HR metrics, addresses employee matters, and collaborates on HR programs and cross-functional initiatives.

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.

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 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.