{"jobs":[{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4697277005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4436726005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4697277005,"updated_at":"2026-05-19T18:33:02-04:00","requisition_id":"564","title":"Biospecimen Data Specialist (Temporary) ","company_name":"Vir Biotechnology","first_published":"2026-05-19T18:33:02-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Bio is looking for a Biospecimen Data Specialist (Temporary) who will be responsible for coordinating and managing biospecimen data related to sample tracking, shipment, and reporting. This role ensures accurate logging of transactions tied to sample management, leveraging platforms such as Smartsheet and Excel to facilitate data integrity and transparency throughout the biospecimen lifecycle.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is located in our San Francisco headquarters with an expectation of at least 3 days per week in office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Log and track all biospecimen transactions, including shipments from central labs to third-party labs, returns to sites, and sample destruction\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain and update central and third-party lab databases to ensure real-time accuracy of sample records\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop, implement, and maintain common sample reporting plans using manual and automated tools (e.g., Excel, Smartsheet, or custom programming solutions)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with laboratory teams and external partners to streamline sample management processes and resolve discrepancies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure compliance with regulatory and organizational data standards for biospecimen handling and documentation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in life sciences, data management, or a related field\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with biospecimen or laboratory data management systems (e.g., Smartsheet, Excel)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with programming or automation for data tracking and reporting preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency in data reporting and database maintenance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with regulatory requirements for biospecimen management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong organizational skills and attention to detail\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to work collaboratively in a multidisciplinary environment\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected hourly range for this position is $40.00 to $45.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4029153005,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4698554005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4437201005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4698554005,"updated_at":"2026-05-22T11:55:25-04:00","requisition_id":"565","title":"Director, Translational Biology ","company_name":"Vir Biotechnology","first_published":"2026-05-21T15:40:17-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Bio is looking for a Director, Translational Biology to drive biomarker strategy across our pipeline, from preclinical discovery through clinical development. Reporting to the VP, Translational Biology, you will translate complex immunologic and molecular insights into actionable plans that inform mechanism of action, dose selection, patient selection, and clinical outcomes in immune-oncology and related disease areas.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You will lead biomarker design and execution for key programs, oversee advanced translational assays in both preclinical models and human samples, and partner closely with discovery, clinical, data science, and external collaborators to deliver high-quality biomarker data. You will manage scientists, contribute to regulatory filings, and help build the infrastructure and partnerships needed to advance cutting-edge biomarker science.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is located in our San Francisco headquarters with an expectation of at least 3 days per week in office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the biomarker lead for specific programs from preclinical through clinical development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and execute biomarker strategies, including design and oversight of preclinical biomarker assessments and contribution to clinical biomarker plans to inform dose selection and development of immune-oncology agents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Plan and oversee the validation and execution of human immunologic and molecular methods in preclinical and clinical studies to meet biomarker objectives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support activities related to deliverables and documentation for regulatory submissions (e.g., INDs, BLAs/NDAs) and contribute to authoring INDs, IBs, clinical study protocols, and related documents\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage pilots and method validation with external vendors to ensure robust, fit-for-purpose biomarker assays\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with discovery, clinical, and data science colleagues to refine biomarker hypotheses, design studies, and analyze and interpret key datasets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead a team, providing scientific guidance and mentorship in immunology and biomarkers while overseeing team performance and development\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent the Research function in selected external meetings, providing scientific input to support partnerships, due diligence, and program evaluations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help develop and manage internal and external resources, including CROs and academic collaborators, to advance biomarker discovery and implementation\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD and 10+ years, or MS and 13+ years, of relevant industry-focused experience in immune-oncology, immunology, or a closely related field, including drug and biomarker development from preclinical through Ph1–3 clinical stages\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record in designing and executing biomarker strategies, encompassing biomarker identification, validation, and characterization in vitro and in vivo to inform mechanism of action, dose selection, and patient stratification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep subject-matter expertise in immunology and immune-oncology\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency with immunology assays (e.g., polychromatic flow cytometry, cytotoxicity, T cell function, antigen presentation, and other in vitro systems)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to develop and implement robust, qualified/validated biomarker methods for clinical use, including oversight of assay pilots and method validation with external vendors/CROs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong background in contributing to regulatory documents in support of translational and clinical programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Familiarity with the development or application of diagnostic or companion diagnostic tests for patient enrichment, selection, or prediction of therapeutic efficacy\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated scientific and people leadership, including managing scientists and leading cross-functional translational or biomarker teams\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected salary range for this position is $207,500 to $261,500 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology\u0026#39;s compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4029152005,"name":"Research","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4703500005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4439484005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4703500005,"updated_at":"2026-06-05T10:50:16-04:00","requisition_id":"570","title":"Executive Assistant (Temporary) ","company_name":"Vir Biotechnology","first_published":"2026-06-05T10:50:16-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology is looking for a Temporary Executive Assistant (EA). In this EA role, you will provide comprehensive administrative support, enabling our leaders to focus on strategic priorities and key initiatives while supporting their teams effectively. You will be responsible for managing a busy and dynamic calendar, coordinating meetings with a wide range of stakeholders, and ensuring smooth day-to-day operations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in our San Francisco, California office with the expectation to be onsite 5 days a week.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Plan, schedule, and coordinate complex meetings and events with internal teams and a wide range of external partners including accommodating scheduling conflicts and last-minute changes\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage highly sensitive and confidential information regarding business strategies, organizational priorities, and key initiatives with discretion\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Help facilitate strong working relationships with internal and external stakeholders. Gather briefing materials for meetings and ensure timely follow-up and consistent communication\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Organize domestic and international travel, including flights, hotels, transportation, and itineraries\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Process expense reports\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support special projects, team initiatives, or event planning as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be the go-to person for day-to-day administrative needs, and problem solving for those you support\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Anticipate needs and help ensure nothing falls through the cracks\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;10+ years’ experience with at least 3+ years supporting either C level executives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in the biotechnology / pharmaceutical industry required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Highly organized, detail-oriented, and able to manage multiple tasks simultaneously\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proactive and resourceful, with strong problem-solving skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Excellent communication skills\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable working in a fast-paced, dynamic environment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Able to maintain a high level of professionalism and confidentiality\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficient in Microsoft Office and calendar management tools (e.g., Outlook)\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected hourly range for this position is $58.00 to $82.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4134325005,"name":"Administrative","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4695551005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4435902005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4695551005,"updated_at":"2026-05-14T14:56:23-04:00","requisition_id":"561","title":"Scientist, Analytical Development Bioassays (Temporary)","company_name":"Vir Biotechnology","first_published":"2026-05-14T14:56:23-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology is looking for a Scientist, Analytical Development (Temporary). You will report to the Director, Analytical Development Bioassays and support the development of bioassays to interrogate the mechanism of action for antibody and other biologic therapeutics. You will execute cell-based and binding assays for characterization testing in support of process and formulation development, comparability and structure-activity relationship studies. You will design and conduct laboratory experiments, author protocols/reports.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is located in our San Francisco headquarters with an expectation of at least 5 days per week in office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop, optimize and qualify cell-based and binding bioassays\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Bring in new assay modalities and technology to the group as needed\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Prepare assay standards, controls, critical reagents, and ensure appropriate system suitability criteria are met\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Perform characterization testing including binding ELISA, Neutralization assays, and effector function assays to support structure-function studies, force degradation studies and BLA-enabling Process and Formulation development studies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Troubleshoot method-related issues internally and at external labs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author study protocols, development/qualification reports and test methods, summarize and verify data for regulatory filings\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor\u0026#39;s degree with 8+ years\u0026#39; of industry experience, Master\u0026#39;s degree with 6+ years\u0026#39; of industry experience, PhD with no industry experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in bioassay method development, transfer and qualification\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in data analysis of bioassays including parallel line analysis and other statistical data analysis for evaluating method performance\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to execute laboratory experiments both independently and with other team members\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Effective at trouble-shooting method-related issues\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience working on multiple projects, adjusting quickly to changes in priorities\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected hourly range for this position is $55.00 to $70.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4029154005,"name":"Technical Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4680607005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4428394005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4680607005,"updated_at":"2026-04-07T18:31:26-04:00","requisition_id":"550","title":"Senior Director, Alliance Management ","company_name":"Vir Biotechnology","first_published":"2026-04-01T17:45:24-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Bio is looking for a Senior Director, Alliance Management, to provide strategic leadership for a portfolio of high‑value external partnerships, including Vir Bio’s commercial hepatitis delta collaboration with Norgine across Europe, Australia, and New Zealand. This role operates with broad autonomy and accountability for alliance performance and value realization.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You will serve as a senior enterprise leader for certain alliances, partnering closely with cross‑functional executives to shape strategy, establish effective governance, and ensure disciplined execution across the alliance lifecycle. This role is accountable for maximizing the strategic, operational, and financial value of their portfolio of partnered assets through proactive leadership, risk management, and issue resolution.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;As the primary executive interface for assigned partners, you will own alliance health, execution against Definitive Agreements (DAs), and long‑term relationship outcomes, including amendment strategy and exit planning.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is located in our San Francisco headquarters with an expectation of at least 3 days per week in office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Provide strategic leadership for a portfolio of alliances spanning clinical collaborations, co‑development partnerships, and commercial agreements, with accountability for overall alliance performance and value delivery.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and lead fit‑for‑purpose governance models; chair and orchestrate joint governance forums and cross‑company teams to align priorities, enable decision‑making, and drive execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and maintain a clear strategic intent and multi‑year operating plan for each alliance, ensuring alignment with Vir Bio’s portfolio strategy and regular communication to senior stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as the senior point of accountability for partner relationships within the assigned portfolio, setting the tone for collaboration, trust, and performance; proactively address relationship risks and escalation topics.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own oversight of financial and non‑financial obligations, including leadership of quarterly partner financial reviews, forecasting, and variance analysis in close partnership with Finance.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure disciplined execution against all contractual obligations, including milestones, payments, supply commitments, and performance terms, with timely identification and mitigation of execution risks.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead partner negotiations related to agreement amendments, extensions, and terminations, in collaboration with Legal, BD, and functional leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Anticipate and manage complex alliance challenges arising from contractual interpretation, strategic misalignment, or operational dependencies, applying sound judgment and enterprise perspective.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive continuous improvement in alliance effectiveness by conducting structured alliance health assessments and translating insights into concrete actions that enhance value realization.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BA/BS with 18+ years, MS/MBA with 16+ years, or PhD with 13+ years of progressive pharmaceutical or life sciences experience in senior leadership roles\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+ years of experience in Alliance Management and/or Partnering within a biotech or pharmaceutical organization, managing complex, high‑value partnerships.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven experience leading alliances involving late‑stage development assets, with additional experience supporting commercial‑stage products and launches.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong command of development, commercialization, and collaboration agreements, with the ability to interpret, negotiate, and operationalize complex contractual terms.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated ability to lead through influence in a highly matrixed environment and to partner effectively with senior executives across functions and organizations.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong strategic, analytical, and problem‑solving capabilities, with consistent application of sound business judgment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative leadership style with the ability to build alignment, drive decisions, and hold teams accountable.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Comfortable operating in a fast‑paced, evolving environment with high ambiguity and enterprise‑level visibility.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience in the fields of infectious diseases and oncology preferred.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected salary range for this position is $227,500 to $318,000 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology\u0026#39;s compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4076176005,"name":"Business Development","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4700564005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4438162005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4700564005,"updated_at":"2026-05-28T18:37:43-04:00","requisition_id":"567","title":"Senior Director, Clinical Development-Infectious Disease ","company_name":"Vir Biotechnology","first_published":"2026-05-28T18:37:43-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology is looking for a Senior Director, Clinical Development-Infectious Disease\u0026amp;nbsp;to facilitate late‑stage clinical development for our\u0026amp;nbsp;hepatitis delta (HDV)\u0026amp;nbsp;portfolio, with a primary focus on activities supporting the\u0026amp;nbsp;Phase III clinical program and health authority submission activities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the VP, Clinical Development, this senior leader will serve as the key clinical voice in shaping and executing the clinical development strategy You will concentrate on advancing our HDV assets through global Phase III,BLA‑enabling activities and support on relevant commercial activities.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is located in our San Francisco headquarters with an expectation of at least 3 days per week in office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead one of our HDV Phase 3 studies for Clinical Development and support the Clinical Development Sub team Lead\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute the late‑stage clinical development plan providing oversight of Phase III studies, incl, including medical monitoring and benefit–risk assessment\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead BLA‑enabling activities and clinical components of global regulatory submissions (e.g., BLA, NDA, MAA) and Health Authority interactions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to the development and execution of a life cycle management strategy, including but not limited to potential post marketing commitments from a clinical development perspective\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Regulatory Affairs, Biostatistics, Data Management, and Medical Writing to ensure clinical datasets, narratives, and summaries meet FDA, EMA, and ICH standards for regulatory filings\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to key clinical and regulatory documents, including protocols, IBs, IND submissions and reports, clinical study reports, and development plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Regulatory Affairs, Biostatistics, Clinical Operations, Safety, Translational Medicine, and Commercial to develop and execute integrated development and registration strategies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Interpret and integrate clinical data across studies and drive preparation of internal decision documents, integrated analyses, and external publications/presentations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build and maintain strong relationships with investigators, KOLs, and advisory boards in infectious diseases\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure adherence to GCP, ICH guidelines, and SOPs, and contribute to continuous improvement of clinical development processes\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;MD, or PharmD/PhD and 8-10+ years of clinical development experience in the biopharmaceutical industry, with infectious disease or hepatology experience.\u0026amp;nbsp; Other therapeutic areas experience(s) may be considered with strong regulatory submission experience.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated late‑stage/registrational experience, including leadership of or major contribution to Phase III programs, and direct experience supporting at least one BLA (or NDA/MAA) submission in a clinical leadership role required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep familiarity with GCP, ICH guidelines, and global regulatory expectations for registrational trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to design and interpret complex Phase II/III clinical trials and integrated clinical packages, and to interact effectively with Health Authorities, KOLs, and internal senior leadership.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience leading cross‑functional teams\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected salary range for this position is $235,500 to $329,500 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology\u0026#39;s compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4029153005,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4687372005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4431605005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4687372005,"updated_at":"2026-04-21T11:58:31-04:00","requisition_id":"553","title":"Senior Director, Clinical Pharmacology and Translational PK/PD","company_name":"Vir Biotechnology","first_published":"2026-04-21T11:58:31-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology is looking for an experienced Sr. Director of Clinical Pharmacology and Translational PK/PD to lead the technical and operational aspects of the department in support of programs across all stages of preclinical and clinical development. You will work across Vir Bio\u0026#39;s portfolio of infectious disease and oncology programs, providing hands-on leadership while managing and developing a team. In this role, you will work collaboratively with internal and external cross-functional teams and consultants to support the successful and timely advancement of drug development programs. You will evaluate and apply best practices and innovative techniques to foster successful execution and outcomes of clinical studies. You will report to the VP of Translational Development.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is located in our San Francisco headquarters with an expectation of at least 3 days per week in office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee clinical pharmacology and translational PK/PD operations and deliverables across all stages of development for both infectious disease and oncology programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent clinical pharmacology and translational PK/PD as technical expert on cross-functional project teams and provide strategic input to program advancement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop fit-for-purpose clinical pharmacology strategies to enable development and regulatory decisions from pre-IND through market authorization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Select and execute appropriate modeling and simulation approaches (PK/PD, PopPK, exposure-response) to inform dose selection, optimization, and justification for Phase 2 and pivotal trials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Author and provide technical input for regulatory documents and submissions (protocols, IBs, briefing packages, INDs, NDAs/BLAs) and responses to questions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Work collaboratively with cross-functional teams, including clinical research, clinical operations, biomarkers, bioanalytical, biometrics, CMC, research, and regulatory in support of program advancement\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish and manage collaborations with external vendors and collaborating partners\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Generate and manage departmental budget(s) and optimize resource allocation across multiple programs\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage and develop the Clinical Pharmacology and Translational PK/PD team, including hiring, mentoring, and building departmental capabilities to support organizational needs\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;PhD, PharmD, or MD with relevant training in clinical pharmacology, pharmacokinetics, pharmaceutics, or related field with 13+ years industry experience in Clinical Pharmacology, DMPK and/or related fields\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Mastery of nonclinical and clinical pharmacokinetic concepts and methodologies with deep understanding of multidisciplinary drug development requirements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in PK/PD, PopPK and exposure-response modeling with proficiency in R and extensive hands-on experience with Monolix or NONMEM\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Extensive experience leading translational and clinical pharmacology work from FIH dose selection through market authorization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong understanding of regulatory requirements and experience contributing to regulatory submissions and engagements\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working knowledge of bioanalytical techniques in support of clinical development of small molecules and biologics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience with biologics, including monoclonal antibodies and bispecifics required; experience in oncology and/or infectious disease indications strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proficiency using standard PK analysis and graphing programs (Phoenix WNL, Graphpad, R, etc.)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to manage and develop teams\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected salary range for this position is $235,500 to $329,500 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology\u0026#39;s compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4030268005,"name":"Product Development","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4696573005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4436384005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4696573005,"updated_at":"2026-05-18T15:44:13-04:00","requisition_id":"562","title":"Senior Director, Clinical Research (Oncology) ","company_name":"Vir Biotechnology","first_published":"2026-05-18T15:44:13-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Senior Director, Clinical Research Oncology will provide strategic and operational leadership for the Clinical Science function within Oncology Clinical Development. You will be accountable for shaping and executing clinical development strategies across oncology programs, ensuring scientific rigor, regulatory alignment, and efficient delivery of high‑quality clinical data.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role requires an experienced MD, PhD or PharmD with deep expertise in oncology drug development and a proven track record of leading clinical research teams through complex development programs, from first‑in‑human through registration.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Clinical Science \u0026amp;amp; Development Leadership\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as the Clinical Science functional leader for one or more oncology programs across early and/or late‑stage development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and drive clinical development strategies, including indication selection, study design, endpoints, and lifecycle planning.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Provide clinical and scientific leadership across all phases of development, including Phase 1, dose expansion, registrational, and post‑approval studies.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ensure integration of clinical, translational, pharmacology, biometrics, and regulatory perspectives into cohesive development plans.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Study \u0026amp;amp; Program Oversight\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Oversee clinical science deliverables for assigned studies, including protocols and amendments, informed consent forms (ICFs), case report form (CRF) design and data review strategies, and clinical study reports (CSRs) as well as the clinical sections of regulatory submissions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Guide ongoing clinical data review, interpretation, and risk assessment, escalating key findings and safety signals as appropriate.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner closely with Clinical Operations to ensure high‑quality study execution, timelines, and decision‑\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;Cross\u0026lt;/u\u0026gt;\u0026lt;u\u0026gt;‑\u0026lt;/u\u0026gt;\u0026lt;u\u0026gt;Functional \u0026amp;amp; Governance Leadership\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Act as the clinical science representative on program teams, clinical development sub‑teams, and governance forums.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive alignment and decision‑making across Clinical Operations, Biometrics, Translational Medicine, Clinical Pharmacology, Regulatory, Safety, and Medical Writing.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Present and defend clinical strategy and data to internal governance committees, executive leadership, and external stakeholders.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;External Engagement\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as a key scientific interface with investigators and key opinion leaders (KOLs), advisory boards and steering committees, and regulatory agencies, as needed.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support preparation for and participation in regulatory interactions and scientific meetings.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;u\u0026gt;People \u0026amp;amp; Functional Leadership\u0026lt;/u\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead, mentor, and develop clinical scientists, fostering scientific excellence, accountability, and career growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to building and scaling the Clinical Science function, including process development, talent strategy, and best practices.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;MD, PhD, or PharmD in a relevant scientific or medical discipline (e.g., Oncology, Immunology, Pharmacology, Molecular Biology).\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;12+ years of experience in oncology clinical research and drug development in a pharmaceutical, biotechnology, academic, or CRO environment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated experience leading both early‑ and late‑stage clinical development programs.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to serve as a clinical science or program lead, with accountability for strategy and execution.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience contributing to or leading regulatory submissions and interactions is strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrate a deep understanding of oncology clinical trial design and execution, GCP/ICH guidelines and regulatory expectations, and clinical data interpretation, safety evaluation, and benefit‑risk assessment.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong knowledge of translational and biomarker strategies that inform clinical development decisions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborative leader with a track record of effective cross‑functional partnership\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected salary range for this position is $235,500 to $329,500 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology\u0026#39;s compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4029153005,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4693885005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4434824005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4693885005,"updated_at":"2026-05-08T14:57:10-04:00","requisition_id":"560","title":"Senior Director, Organizational Design ","company_name":"Vir Biotechnology","first_published":"2026-05-08T14:57:10-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology is looking for a Senior Director, Organizational Design, who will be responsible for leading organizational design and effectiveness strategies that support Vir Bio’s mission during an exciting period of evolution in the company’s growth. This role will report to the Head of HR.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Operating at the intersection of talent strategy, workforce planning, and enterprise transformation, this role partners closely with senior leaders, HR Business Partners, and cross-functional stakeholders to identify, build, and enable scalable workforce solutions.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This leader will bring data-informed insights, strong facilitation skills, and pragmatic change leadership to complex, high-stakes business challenges typical of a rapidly scaling immuno-oncology organization. You will develop OD strategies that reinforce Vir Bio’s patient-focused, high-accountability culture.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The role will provide expert technical expertise, facilitation and advisory support while ensuring business leaders and HRBPs retain clear accountability for business decisions, execution and outcomes.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is located in our San Francisco headquarters with an expectation of at least 3 days per week in office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Organizational Design \u0026amp;amp; Effectiveness\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead organizational design initiatives and operating model evolutions across functional and matrixed teams.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support senior leaders and HRBPs in diagnosing organizational effectiveness challenges and suggest solutions.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;In close partnership with HRBPs, Finance, and business leaders, translate business and scientific roadmaps into workforce implications and scenarios.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define and evolve enterprise workforce architecture standards (e.g., role clarity, capability models, span/layer principles)\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Build tools and develop insights enabling proactive workforce planning that integrates into long-range talent processes; ensure the organization scales ahead of demand rather than reactively.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Change Management \u0026amp;amp; Organizational Readiness\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Develop change management strategies for OD and organizational effectiveness initiatives.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Act as a trusted advisor during periods of ambiguity, transformation, and rapid growth.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Assess organizational health and readiness for change, partner with HRBPs and business leaders to support teams through transitions.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Data, Insights \u0026amp;amp; Measurement\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Establish metrics and diagnostics to assess organizational effectiveness.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with HR and business leaders to translate insights into clear narratives and options that influence decision-making at the enterprise level.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Track impact of OD/OE initiatives to inform continuous improvement and organizational learning.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Capability Building \u0026amp;amp; Scaled Solutions\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Build and deploy scalable and self-sustaining OD/OE frameworks and resources including digital and AI-enhanced tools.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with other HR COEs to integrate OD/OE practices into the HR operating model including talent reviews, succession planning, and leadership development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain a strong external network (coaches, facilitators, researchers) to supplement internal capability as needed.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree required; advanced degree (e.g., MBA, OD, I/O Psychology, HR or related field) strongly preferred.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;12–15+ years of progressive experience in organizational design, organizational effectiveness, talent strategy, workforce transformation, or internal consulting.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience supporting late-stage or commercial-stage biotech/pharma organizations with a focus on oncology or immuno-oncology required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated success partnering with senior leaders on complex, enterprise-level organizational challenges.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep expertise in organizational design, team effectiveness, leadership development, and change management.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong facilitation, coaching, and executive influence skills; executive coaching certification and/or substantial coaching experience is a plus.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Enterprise mindset with the ability to connect organizational decisions to scientific, clinical, and commercial outcomes.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven ability to build trusting, collaborative partnerships with diverse stakeholders across functions and levels.\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected salary range for this position is $227,500 to $318,000 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology\u0026#39;s compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4029156005,"name":"Human Resources","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4700555005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4438160005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4700555005,"updated_at":"2026-05-28T18:20:47-04:00","requisition_id":"566","title":"Senior Manager, Quality Control ","company_name":"Vir Biotechnology","first_published":"2026-05-28T18:20:47-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The Senior Manager, Technical Operations Quality Control, is responsible for executing and operationalizing QC strategy across assigned programs and external testing partners (e.g., CDMOs/CTLs) from Phase 1 through commercialization. This role ensures the timely and compliant delivery of QC activities, including release and stability testing, method lifecycle management, and vendor oversight.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The Senior Manager partners cross-functionally with Quality, Technical Operations, Regulatory, and Analytical Development to deliver program milestones, maintain inspection readiness, and support global regulatory submissions. This individual contributes to the development of QC strategy and drives continuous improvement in QC processes, systems, and external network performance.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is located in our San Francisco headquarters with an expectation of 3 days per week in office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Execute and operationalize QC strategy for assigned programs and external testing networks in alignment with QC and Quality organization strategy.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead QC activities across the product lifecycle (Phase 1 through commercial) for designated programs, ensuring effective implementation of phase-appropriate control strategies.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Support development and refinement of QC strategies, including methods, specifications, and testing approaches, in collaboration with Analytical Development and QC leadership.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive consistent execution and harmonization of QC methods, specifications, and practices across programs and external partners.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026amp;nbsp;Identify, assess, and escalate risks to QC performance, supply continuity, and compliance, and implement mitigation plans with cross-functional stakeholders.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Represent QC on program teams and sub-teams, ensuring alignment of analytical deliverables, timelines, and QC readiness for key CMC milestones.\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage day-to-day execution of QC operations to ensure\u0026amp;nbsp;timely, compliant testing for clinical and commercial programs.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate and oversee release and stability testing (including CDMOs/CTLs), including review of analytical data, batch records, and supporting documentation; support CoA generation.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead execution of QC GMP processes (deviations, OOS/OOT, change controls, investigations) in collaboration with QA.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coordinate QC documentation and\u0026amp;nbsp;logistics\u0026amp;nbsp;at external labs, including sampling plans, shipments, and reagent/inventory management.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Manage vendor performance and execution, including CTL/CDMO oversight and routine operational interactions.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Execute\u0026amp;nbsp;method\u0026amp;nbsp;lifecycle activities (qualification, transfer, validation, implementation, and monitoring) across internal and external labs.\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BA/BS with 10 + years experience, MA/MS/MBA with 8+ years experience in Biochemistry, Chemistry, Biology, Virology, Chemical Engineering or a related discipline is preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Technical expertise in a wide range of analytical methods for release and stability testing of monoclonal antibodies\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong scientific background in Quality Control and/or assay development in biotech industry with strong knowledge of cGMP/ICH/FDA/EMA regulations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise with analytical test method optimization, validation, and transfer as well as working with contract organizations\u0026amp;nbsp;\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected salary range for this position is $142,500 to $199,000 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology\u0026#39;s compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4029154005,"name":"Technical Operations","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4678398005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4427336005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4678398005,"updated_at":"2026-03-27T12:54:33-04:00","requisition_id":"549","title":"SVP, Oncology Therapeutic Area Head","company_name":"Vir Biotechnology","first_published":"2026-03-27T12:54:33-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Reporting to the Chief Medical Officer, or CMO, the SVP Oncology Therapeutic Area Head, or TA Head, will be responsible for overseeing the successful development of multiple molecules for the treatment of cancer in Vir Biotechnology\u0026#39;s oncology portfolio. The Oncology TA Head will lead the oncology strategy and lead a cross-functional clinical team to develop novel therapeutics from IND through marketing application and registration.\u0026amp;nbsp; This will include guidance and oversight of clinical development strategies for multiple programs and provision of expert input to clinical developability of pre-clinical assets in the oncology pipeline.\u0026amp;nbsp; The TA head will be a key partner for the Research Organization and will provide clinical and strategic leadership for programs in Discovery through IND filing.\u0026amp;nbsp; The TA Head will also be a key partner for business development in oncology.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is located at Vir Bio’s San Francisco headquarters with an expectation of 3 days per week in the office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead Vir Bio\u0026#39;s Oncology clinical development strategy to deliver registrational data to health authorities for evaluation and, ultimately, to patients and the oncologists who care for them.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee activities to ensure appropriate objectives and resources are deployed to deliver on key milestones to advance the company’s oncology assets in development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Coach and mentor program team leaders, clinical scientists and medical monitors.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Regulatory Sciences to shape the regulatory strategy for oncology clinical development programs and play a key role in representing the Company in health authority interactions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Core member of the CMO Organization Leadership Team\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Responsible for collaborating with stakeholders across Vir Bio and with external partners, including potential joint development steering committees, to shape the strategy and efficient advancement of molecules throughout clinical development.\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;At major congresses, and as needed, represent the Company and the science to various internal and external stakeholders (including the Board of Directors, clinical investigators, KOLs, patient advocacy groups, investors, and analysts).\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;A highly experienced, collaborative, and innovative leader with extensive clinical drug development experience will thrive in this role.\u0026amp;nbsp; A successful candidate will demonstrate strategic and technical prowess, build strong working relationships, and have an entrepreneurial spirit.\u0026amp;nbsp; Specific qualifications include:\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;M.D. with specialty training in Oncology required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Minimum 12+ years of experience in early and late-stage clinical development at biotech or pharmaceutical company required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated track record applying strategic context to development planning, ability to balance risk and make trade-offs to advance the portfolio priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;A high degree of business acumen, a big-picture perspective, and the ability to galvanize a team around a common goal\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated track record of accountability, scientific rigor, and innovation\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Ability to build teams and a culture that nourishes creativity, scientific curiosity, with integrity and respect across functions and layers within the Company\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;An outcome-driven mindset and a commitment to achieving key milestones\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Exceptional interpersonal and communication skills able to clearly convey complex medical and scientific information to a wide range of internal and external audien\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology\u0026#39;s compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4029153005,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4702094005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4438856005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4702094005,"updated_at":"2026-06-02T18:41:34-04:00","requisition_id":"569","title":"Vice President, Clinical Research-Infectious Disease","company_name":"Vir Biotechnology","first_published":"2026-06-02T18:41:34-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology seeks a Vice President of Clinical Research to set strategy and lead the development of multiple programs across our infectious disease portfolio, including our Hepatitis Delta program currently in Phase III and BLA‑enabling activities. You will lead the planning, design, and oversight of clinical studies from preclinical through Phase IV and commercialization, with immediate responsibility for advancing our Hepatitis Delta program through registration.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Working with internal colleagues and external partners, you will inform target and indication selection and shape clinical strategies. You\u0026#39;ll partner with research scientists and external experts to refine development plans and stay current with advances in the field. You\u0026#39;ll collaborate with Development Operations, Regulatory, Biometrics, and other functions to oversee trial design and execution.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You’ll thrive in this role if you’re a collaborative, scientifically grounded clinical development leader with a hands‑on, team‑oriented approach. You will lead a team of clinical physicians and scientists while serving as a key influencer across the organization.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is located in our San Francisco headquarters with an expectation of at least 3 days per week in office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Serve as a strategic clinical leader, shaping creative and efficient development strategies for multiple pipeline assets\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;\u0026amp;nbsp;Lead clinical research sub‑teams through direct management of MDs and clinical scientists\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead regulatory interactions to advance molecules through development and secure global regulatory approvals\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with relevant functions to ensure strategic integration of product development plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Oversee all major written deliverables (protocols, clinical sections of regulatory submissions, publications, abstracts) and presentation materials\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Collaborate with Research and Translational Development to identify drug targets and disease indications, and shape clinical development plans\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Be accountable for all relevant timelines and deliverables\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a key spokesperson at external meetings, including regulatory and scientific forums\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;MD, DO, or PharmD with a strong research background; specialty training in Infectious Diseases preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;8+\u0026amp;nbsp;years of progressive clinical development experience with a strong record of strategic trial design, late‑stage execution, and cross‑functional leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record leading registrational trials and marketing applications (NDA/BLA/MAA) through to approval required\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep experience in regulatory interactions with global health authorities, including leading filing strategy and submissions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Current working knowledge of legal, regulatory, and compliance regulations and guidelines; strong understanding of clinical trial design, execution and statistics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adaptable and able to effectively lead, collaborate and influence across a complex matrix organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated leadership in ambiguous situations; able to inspire a team to excel by fostering a climate of energy, excitement and personal accountability\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected Salary range for this position is $320,000 to $410,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology\u0026#39;s compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4029153005,"name":"Development","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4701442005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4438457005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4701442005,"updated_at":"2026-06-01T12:10:22-04:00","requisition_id":"568","title":"Vice President, Finance Planning and Analysis ","company_name":"Vir Biotechnology","first_published":"2026-06-01T12:10:22-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Bio is seeking a Vice President of Financial Planning \u0026amp;amp; Analysis to lead enterprise‑wide financial planning and serve as a core member of the Company’s strategic and operational leadership. This role is accountable for driving capital allocation, long‑range financial strategy, and performance management across the organization, with direct impact on enterprise value creation and strategic decision‑making.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;The VP, FP\u0026amp;amp;A will own the Company’s planning and forecasting architecture, valuation framework, and financial decision support, partnering closely with the executive team, functional leadership, and project teams. This is a highly visible, hands‑on leadership role requiring strong judgment, deep biotech financial expertise, and the ability to translate complexity into clear, actionable recommendations.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is based in Vir’s San Francisco headquarters with an expectation of at least three days per week in the office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the enterprise FP\u0026amp;amp;A function, establishing short‑ and long‑term financial plans that align capital deployment with the Company’s highest‑value strategic priorities\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Own company‑wide budgeting, forecasting, and long‑range planning processes, with accountability for performance against plan and recommended corrective actions\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Serve as a senior finance business partner to executive leadership, providing financial leadership on clinical development, manufacturing, partnerships, commercial and key strategic initiatives\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Partner with Accounting on collaboration and partnership financials, including quarter‑end activities, external funding applications, reporting, and partner‑facing budget management\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Maintain and continuously refine the Company’s internal valuation and scenario‑modeling framework\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Lead, develop, and scale a high‑performing FP\u0026amp;amp;A team responsible for portfolio investment analysis and strategic financial support for R\u0026amp;amp;D\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Advance financial analytics, reporting, and systems to support executive, Board, investor, and partner decision‑making along with assisting with internal and business development valuations\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and implement process and reporting enhancements that improve transparency, discipline, and decision quality\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Bachelor’s degree in finance, accounting, or a related discipline, with fifteen or more years of progressive finance leadership experience\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;MBA and/or CPA, or equivalent advanced credentials strongly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Deep experience supporting biotech or pharmaceutical R\u0026amp;amp;D organizations, including development economics and portfolio decision‑making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Demonstrated expertise in valuation, scenario modeling, and capital allocation in complex and uncertain environments\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Commercial financial planning expertise in the Biotech or Pharma industry\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven executive leadership skills, including building and leading teams, influencing senior stakeholders, and partnering cross‑functionally\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Strong systems orientation with experience operating sophisticated planning, forecasting, or ERP platforms\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Sound knowledge of US GAAP, internal controls, and SOX‑compliant environments\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected salary range for this position is $300,000 to $350,000. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology\u0026#39;s compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4029155005,"name":"Finance","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]},{"absolute_url":"https://job-boards.greenhouse.io/virbiotechnologyinc/jobs/4688224005","data_compliance":[{"type":"gdpr","requires_consent":false,"requires_processing_consent":false,"requires_retention_consent":false,"retention_period":null,"demographic_data_consent_applies":false}],"internal_job_id":4432004005,"location":{"name":"San Francisco, California, United States"},"metadata":null,"id":4688224005,"updated_at":"2026-04-23T11:10:03-04:00","requisition_id":"555","title":"Vice President, Strategy and Portfolio Planning ","company_name":"Vir Biotechnology","first_published":"2026-04-23T11:10:03-04:00","language":"en","application_deadline":null,"content":"\u0026lt;div class=\u0026quot;content-intro\u0026quot;\u0026gt;\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt; dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology has exclusive rights to the universal PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;masking platform for oncology and infectious disease. PRO-XTEN\u0026lt;sup\u0026gt;®\u0026lt;/sup\u0026gt;\u0026amp;nbsp;is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;/p\u0026gt;\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;THE OPPORTUNITY\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology seeks a Vice President, Strategy \u0026amp;amp; Portfolio Planning, reporting to the Chief Business Officer, who will be responsible for guiding the company\u0026#39;s strategy and optimizing its portfolio of programs products, and partnerships. This visible leadership position works across all business units.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You will serve as a thoughtful strategic partner to the CBO and executive leadership team, driving corporate strategy and portfolio prioritization. You will optimize Vir Bio\u0026#39;s business, translate enterprise-level strategies into actions, and align the organization to the strategy. Working closely with competitive intelligence, business development, and alliance management CBO sub-teams, you will develop Vir Bio\u0026#39;s long-term strategic plan and lead integrated asset-level strategies across clinical and preclinical-stage programs. An enterprise leader, you will apply analytical rigor, translate complex clinical, scientific, and financial data into clear recommendations, articulate strategy, and work collaboratively across the company.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;You’ll thrive in this role if you love shaping big-picture strategy in fast-moving biotech environments, get energized by steering clinical-stage portfolios to provide the greatest patient benefit, and leveraging your experience across organizations both large and small.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This role is in our San Francisco headquarters with at least 3 days per week in the office.\u0026lt;/p\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHAT YOU\u0026#39;LL DO\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Corporate Strategy\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Lead the development and evolution of Vir Bio\u0026#39;s long-term strategic plan in partnership with the CBO, executive leadership, and Board of Directors\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Adapt corporate strategy in response to emerging clinical data, evolving market dynamics, and competitive landscape shifts\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Working closely with the CEO, CBO, and CEO Chief of Staff, conceptualize and create board materials for quarterly board meetings and strategic offsites\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Drive scenario planning and options analysis to inform critical business decisions and enable agile executive team decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Contribute to investor communications and narratives supporting company growth\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Design and manage strategic planning cycles, leadership meetings, and governance forums to enable clear priorities, decision-making, and execution tracking\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;p\u0026gt;\u0026lt;strong\u0026gt;Portfolio Planning\u0026amp;nbsp;\u0026amp;nbsp;\u0026lt;/strong\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;Partner with the CBO and executive leadership to shape Vir Bio\u0026#39;s long-term portfolio strategy, evaluating diversification pathways and strategic options under different capital, partnership, and market scenarios\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Define portfolio strategy frameworks and valuation methodologies (NPV analysis, risk-adjusted valuations, scenario modeling) that inform corporate development priorities, investment decisions, and strategic prioritization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Develop and implement analytical frameworks and decision-making tools (including those leveraging AI/ML) that enhance organizational capabilities, driving data-driven strategic maturity and alignment across the organization\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Conduct portfolio-level strategic analysis to identify gaps, optimize risk profile, and maximize financial returns, influencing business development target identification and deal thesis development in close partnership with senior leadership\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Establish portfolio metrics, KPIs, and measurement frameworks to evaluate performance against strategic objectives, integrating competitive intelligence, emerging clinical data, and market insights into decision-making\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Engage external advisors, consultants, and KOLs to inform portfolio strategy and validate strategic assumptions\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO YOU ARE AND WHAT YOU BRING\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;ul\u0026gt;\n\u0026lt;li\u0026gt;BA/BS with 20+ years, MS/MBA with 18+ years, or PhD with 15+ years of progressive pharmaceutical or life sciences experience in senior leadership roles; experience in infectious disease and/or oncology highly preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Proven track record in corporate strategy development, portfolio management, and strategic execution within or for large and small biopharmas\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Biopharma strategy consulting experience, preferably with one of the premier management consulting firms preferred\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience leading integrated strategy across clinical-stage programs, including portfolio prioritization, development planning, and commercial positioning\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Expertise in financial modeling, valuation methodologies (DCF, NPV, risk-adjusted valuations), and portfolio analytics\u0026lt;/li\u0026gt;\n\u0026lt;li\u0026gt;Experience delivering strategic initiatives through governance processes and managing ambiguity\u0026lt;/li\u0026gt;\n\u0026lt;/ul\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;div class=\u0026quot;section page-centered\u0026quot;\u0026gt;\n\u0026lt;div\u0026gt;#LI-AS1\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;#LI-Onsite\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\u0026amp;nbsp;\u0026lt;/div\u0026gt;\n\u0026lt;div\u0026gt;\n\u0026lt;h3\u0026gt;\u0026lt;strong\u0026gt;WHO WE ARE AND WHAT WE OFFER\u0026lt;/strong\u0026gt;\u0026lt;/h3\u0026gt;\n\u0026lt;p\u0026gt;The expected salary range for this position is $300,000 to $350,000 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology\u0026#39;s compensation and benefits are aligned with the current market and commensurate with the person’s experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;div class=\u0026quot;content-conclusion\u0026quot;\u0026gt;\u0026lt;div class=\u0026quot;content-wrapper posting-page\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;content\u0026quot;\u0026gt;\n\u0026lt;div class=\u0026quot;section-wrapper page-full-width\u0026quot;\u0026gt;\n\u0026lt;p\u0026gt;Applicants must currently be authorized to work for any employer in the U.S.\u0026amp;nbsp; We are unable to sponsor or take over sponsorship of an employment Visa at this time.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs.\u0026amp;nbsp; Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.\u0026lt;/p\u0026gt;\n\u0026lt;p\u0026gt;For hires based in the United States, Vir Biotechnology, participates in \u0026lt;a href=\u0026quot;https://www.e-verify.gov/sites/default/files/everify/posters/EVerifyParticipationPoster.pdf\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;E-Verify\u0026lt;/a\u0026gt;.\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026lt;a href=\u0026quot;https://www.vir.bio/candidate-notice/\u0026quot; target=\u0026quot;_blank\u0026quot;\u0026gt;Candidate Privacy Notice\u0026lt;/a\u0026gt;\u0026lt;/p\u0026gt;\n\u0026lt;p class=\u0026quot;section page-centered\u0026quot;\u0026gt;\u0026amp;nbsp;\u0026lt;/p\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\n\u0026lt;/div\u0026gt;\u0026lt;/div\u0026gt;","departments":[{"id":4076176005,"name":"Business Development","child_ids":[],"parent_id":null}],"offices":[{"id":4011254005,"name":"San Francisco, CA","location":"San Francisco, California, United States","child_ids":[],"parent_id":null}]}],"meta":{"total":14}}