Vir Biotechnology

57 job(s) at Vir Biotechnology

Vir Biotechnology SAN FRANCISCO, CA
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Job Summary:Vir Biotechnology is seeking a candidate to be a trusted business partner to support outsourcing needs for the research service organization focused on vendor selection, contract and vendor management. The candidate will have a proven ability to work collaboratively within a matrix environment to support vendor outsourcing activities. They will partner closely with the outsourced research services team to implement new or improved standards, processes, tools and strategies to enable effective outsourcing of services to vendor partners RESPONSIBILITIES AND LEARNING OPPORTUNITIES:·       Leading the vendor selection lifecycle including Request-for-Information (RFI) and/or Request-for-Proposal (RFP) activities for outsourced research services such as toxicology, DMPK, bioanalytical services, compound screening, cell generation, custom plasmids etc.  ·       Contract lifecycle management (drafting, negotiating, executing, tracking, archiving) of vendor agreements including budget and payment terms in accordance to Vir standards and processes. ·       Loading contract financial terms into a structured format to enable efficient review and comparisons of proposals, negotiation of scope and to enable future-state analytics / reporting. ·       Defining and measuring outcome-based key performance indicators (KPIs) for critical service categories. ·       Developing and maintaining strategic partnerships with key vendors to enable effective collaboration and issue resolution. ·       Consistently communicating status of deliverables with internal and external business partners.·       Supporting the budget forecasting activities and quarterly financial reviews with Corporate Finance. ·       Effectively partnering with relevant internal and external stakeholders such as, Legal, Regulatory, Finance, Quality Assurance and/or vendors, as applicable, to enable informed, risk-considered decisions. ·       Proactively identifying, defining and implementing new or improved Departmental processes or standards. QUALIFICATIONS AND EXPERIENCE:·       8+ years of relevant experience and a B.A./B.S. degree or 5+ years of relevant experience with an advanced degree.  ·       Ability to systematically analyze complex problems, draw relevant conclusions and implement appropriate solutions. ·       Ability to be nimble and to work in ambiguity, as necessary, but also willing and able to follow organizational standards and processes where established.·       Willingness and ability to define, advocate and implement new ideas and solutions to increase the efficiency and effectiveness of the Department / Organization.  ·       Excellent negotiation and persuasion skills, both in one-on-one and group settings. ·       Strong verbal and written skills, and ability to convey complex information in a way that others can readily follow. Vir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. VIR Biotechnology is seeking a Manager, Biosample Operations candidate to support the development portfolio, and is responsible for the development and delivery of biosample strategies across multiple programs and ensures the execution in accordance with regulatory and ethical guidelines. Accountable for planning, organizing, overseeing shipment, and destruction of biosamples from investigator sites or Central Labs and their subsequent delivery to assay laboratories to ensure timely delivery and optimal analyzable quality. Manage long-term archival of samples with respect to regulatory strategic, and/or biochemical limitations. RESPONSIBILITIES & LEARNING OPPORTUNITIES:Develop and implement a global strategy for standardization of clinical sample management for inspection readiness including development of SOPs for consistent practices across clinical programs. Develop the strategy for scalable sample storage, tracking, and access. Ensure the timely and efficient delivery of all biosamples, including scheduling analyses with relevant vendors, sample processing and shipment, and data delivery and final sample disposition.QUALIFICATIONS & EXPERIENCE:Preferred Bachelor’s degree in Life Sciences or equivalent with 8+ years’ experience, Master’s degree with 6+ years’ experience, PhD with 3+ years’ experienceFamiliar with and able to operate consistent with GCP and regulatory requirements. Proven clinical development experience of working in teams running human clinical studies (phase I-IV), monitoring clinical studies or experience of working in clinical studies at an investigator site. #LI-RemoteVir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking a Senior Manager, Medical Affairs to be part of a growing team in support of Vir’s products in the overall development and management of the day-to-day activities of the department.  The Senior Manager will work in a matrixed environment with a diverse range of activities with alliance, inter-, and intra-departmental collaborations to achieve respective department goals and deliverables. The role will encompass aspects of medical affairs strategy, publications, grants management, advisory boards, medical information, field support, conference planning, and training. This position is reporting to the Vice President, Medical Affairs.RESPONSIBILITIES AND LEARNING OPPORTUNITIESFacilitate, manage, and document reviews and approvals of materials (e.g. standard response letters, manuscripts, congress publications, presentations)Provide project management support as needed for specific publication activities, advisory boards, and journal clubsExpand and maintain a library of key manuscripts and as a publication repositoryConduct literature reviews to maintain an up-to-date library, support journal clubs, add applicable updates to therapeutic area-specific newsletters, to share publication alerts,  and monitor for pertinent guideline changesAssist in the development, enhancement and implementation of departmental standard operating procedures and policies, processes, and software systems Assist with the development, review, and maintenance of product and disease-related content (e.g. slides, standard responses, and FAQs) Support Medical Affairs activities at national and international congresses Assist with proposals and contract executionQUALIFICATIONS AND EXPERIENCEPreferred bachelor of science, or related discipline, degree with 10 years of pharmaceutical industry experience, a Master’s degree with 8+ years of experience, or a  PharmD/PhD with 5+ years of experienceRequired 2+ years of Medical Affairs with experience in medical information, standard response letters, medical educational programs, field medical support, publication programs and review committeesAdept at forming and maintaining a collaborative work environment in and among cross-functional teamsProficiency with industry standard software platforms, including DataVision, Veeva, Slack and BoxExperience managing vendors and projects is preferredUnderstanding of the legal and regulatory environment of pharmaceutical industry desiredCross functional experience in product launch setting desiredVir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking an Associate Director of Publication, Medical Affairs, working within a matrix environment, to develop and support the global publication processes and activities within the department of Research. This position will report to the Director of Publications, Medical Affairs. RESPONSIBILITIES AND LEARNING OPPORTUNITIESLead a publication committee and develop a Research publication plan to align with therapeutic publication plansMaintain and adhere to the company’s standard operating procedures for publicationsCoordinate, facilitate, and support Research’s publication activities from concept to content development to reviews to publishingWork with Medical Affairs operations to maintain research publications budget Collaborate cross-functionally within Research, internal stakeholders, alliance partners and external authors to execute medical publication activitiesTrack publications metrics and communicate publication updates to relevant key stakeholders to facilitate ongoing functional and regional planningQUALIFICATIONS AND EXPERIENCEBS/BA with 12 plus years of experience OR MA/MS/MBA with 8 plus years of experience OR PhD/PharmD with 7 years of biopharmaceutical industry experience preferred5 years of publication planning/execution (or related) experience requiredSolid understanding of publication guidances (including ICMJE, GPP3, Consort Guidelines, AMA Manual of Style, among others) and congress/journal requirements for publications requiredAbility to synthesize, interpret, present, and discuss complex medical and scientific dataWorking knowledge of clinical trial design, biostatistics, and standard editorial style conventions preferredResearch experience in virology, immunology or a related field preferredFamiliarity with regulatory and legal guidelines regarding publication planning and strategyRelevant professional certification/credential (i.e., CMPP, AMWA) is a plusVir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology SAN FRANCISCO, CA
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Bio is seeking an experienced Clinical Research Director to support our respiratory program.  Reporting to SVP of Clinical Research, this is a crucial position at Vir. You will play a key role at all stages of product development, focusing on the early-stage development program through global product registration for COVID, Influenza, and other respiratory infections.RESPONSIBILITIES:Responsible for scientific aspects of conceptualizing and planning clinical trials and ensuring cross-functional integration, co-ordination and alignment to enable effective and efficient formulation of development plans, study designs, and clinical study protocolsRepresent clinical research in relevant sub-teams (eg, study management team)Work collaboratively with regulatory and other functions to deliver the clinical research components in the preparation/review of regulatory documents, IND annual reports, IND safety reports, and investigator brochuresProvide ongoing medical and data monitoring for clinical trials including, but not limited to, assessment of eligibility criteria, toxicity management and drug safety surveillanceEnsure adherence to regulatory requirements of study conduct and industry standards of ICH/GCP and internal SOPsCoordinate the collection and assimilation of ongoing data for internal analysis and review. Serve as part of a team responsible for managing the preparation and/or review of data listings, summary tables, study results, study reports, and clinical NDA sections, as applicablePrepare scientific information for presentations to senior management, regulatory agencies, scientific conferences, clinical study investigator meetings, and scientific advisory boardsWork collaboratively with other functions to develop publication strategies and develop manuscripts for publication in peer-reviewed journalsServe as part of a team responsible for defending the clinical development program before regulatory authoritiesServe as a scientific and clinical resource within Vir Clinical ResearchProvide scientific and clinical guidance to other relevant functions (eg, research, toxicology, clinical pharmacology, development operations, regulatory, project management, etc)As appropriate, assist in the clinical evaluation of business development opportunities and provide clinical assessments of relevant drug discovery projectsQUALIFICATIONS AND EXPERIENCE:3+ years’ experience preferred in pharmaceutical industry with a proven success record in clinical research studies and trial designFamiliarity with infectious diseases and/or pulmonary or immunology medicine preferredExperience in conducting global clinical trial programs preferredBasic understanding of ICH/GCP guidelines, FDA and EMEA regulations Direct experience in the strategic and tactical implementation of drug developmentAbility to think analytically and strategically to formulate, develop, and execute clinical plansAbility to work effectively in a multidisciplinary team to cultivate an inclusive environment of respectful, open, and honest dialogue and to foster a robust sharing of ideas and creative problem solvingExperienced with engaging internal and external experts in constructive scientific and clinical dialog around study design, study conduct, and interpretation of clinical resultsWell-developed sense of integrity, strong work ethic, scrupulous attention to detail, clear ability to establish and maintain timelines, and persistent commitment to ensuring a high level of qualityAbility to travel domestically and internationally to company, scientific, regulatory, investigator, and other meetingsEDUCATION:MD (or non-US equivalent of M.D. degree) or with sub-specialization in Internal Medicine/Infectious Diseases, or Pulmonary or related fields preferred with 5+ years of experience; PharmD or PhD candidates with 10+ years of extensive clinical research and drug development experience may be consideredVir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology SAN FRANCISCO, CA
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking an associate director in clinical research to support our HBV functional cure program. This position is reporting to the HBV clinical research lead.  RESPONSIBILITIES AND LEARNING OPPORTUNITIES:Responsible for supporting the scientific aspects of conceptualizing and planning clinical trials and ensuring cross-functional integration, co-ordination and alignment to enable effective and efficient formulation of development plans, study designs, and clinical study protocolsRepresent clinical research in relevant sub-teams (eg, study management team)Work collaboratively with regulatory and other functions to deliver the clinical research components in the preparation/review of regulatory documents, IND annual reports, IND safety reports, and investigator brochuresProvide ongoing medical monitoring for clinical trials including, but not limited to, assessment of eligibility criteria, toxicity management and drug safety surveillanceEnsure adherence to regulatory requirements of study conduct and industry standards of ICH/GCP and internal SOPsServe as part of a team responsible for leading the preparation and/or review of data listings, summary tables, study results, study reports, and clinical sections of regulatory submissions, as applicablePrepare scientific information for presentations to senior management, regulatory agencies, scientific conferences, clinical study investigator meetings, and scientific advisory boards, under the supervision of the HBV clinical leadWork collaboratively with other functions to develop publication strategies and develop manuscripts for publication in peer-reviewed journalsServe as a scientific and clinical resource within Vir Clinical ResearchProvide scientific and clinical guidance to other relevant functions (eg, research, toxicology, clinical pharmacology, development operations, regulatory, project management, etc)QUALIFICATIONS AND EXPERIENCE:Clinical and/or basic research experience with evidence of scientific productivity through grants, authorship, or manuscriptsFamiliarity with infectious diseases and/or clinical Liver Disease medicine is preferredBasic understanding of ICH/GCP guidelines, FDA and EMEA regulations Ability to think analytically and strategically to formulate, develop, and execute clinical plansAbility to work effectively in a multidisciplinary team to cultivate an inclusive environment of respectful, open, and honest dialogue and to foster a robust sharing of ideas and creative problem solvingExcellent scientific written and oral communication skillsExperienced with engaging internal and external experts in constructive scientific and clinical dialog around study design, study conduct, and interpretation of clinical resultsWell-developed sense of integrity, strong work ethic, scrupulous attention to detail, clear ability to establish and maintain timelines, and persistent commitment to ensuring a high level of qualityAbility to travel domestically and internationally to company, scientific, regulatory, investigator, and other meetingsEDUCATION:MD, DO or non-US equivalent of M.D. degree with sub-specialization in Infectious Diseases preferred; PharmD candidates with 7+ years clinical research and drug development experience in infectious diseases and/or liver diseases may be consideredVir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Bio is seeking a Senior Manager, Clinical Operations, responsible for the execution of Phase 1-3 clinical trials including study set-up and execution, vendor management and sponsor oversight activities. Activities will include vendor selection and management, protocol and study documents development, study start-up, maintenance, and closure.RESPONSIBILITIES AND LEARNING OPPORTUNITIESIs responsible for the direction, planning, execution, and interpretation of clinical trials research, data collection activities and clinical operations.Leads implementation of clinical protocols, data collection systems and clinical study reports.Support new and ongoing clinical trials and leads cross functional study teams.Lead clinical and regulatory filesProvides oversight and management of investigational sites, clinical consultants, Contract Research Organizations and other vendors.Selects, develops and evaluates personnel and vendors to ensure the efficient operation of the function.Manages direct report(s) and development of junior team membersQUALIFICATIONS AND EXPERIENCEBS/BA with preferred 10 plus years of experience OR MA/MS/MBA with preferred 8 plus years of experience OR PhD with preferred 5 plus years of experienceExperience in managing clinical studies in all phasesExperience with compound lifecycle from IND to NDAThorough understanding of FDA, EMEA, and ROW ICH and GCP guidelines, as well as thorough understanding of cross-functional clinical processes including and not limited to data management, biostatistics, medical monitoring, drug safety, and regulatory affairsExperience with regulatory compliance audits and inspectionsVir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology SAN FRANCISCO, CA
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking a Manager, Clinical Operations, responsible for the execution of Phase 1-3 clinical trials including study set-up and execution, vendor management and sponsor oversight activities.  Activities will include vendor selection and management, protocol and study documents development, study start-up, maintenance, and closure. Candidate will lead cross functional study teams and may manage direct reports.RESPONSIBILITIES & LEARNING OPPORTUNITIES:RFP process, study contract/budget development, and study forecast/planning including timelinesManage CRO, central lab, systems vendors, and ancillary vendors to ensure on target deliverablesDevelop study plans and relevant study document templates for study teamsStrategic input and leadership in study set-up and executionManage team with direct reports within therapeutic areaLead cross functional study teams Main point of contact for operational day-to-day activitiesStakeholder management with internal business partners, key opinion leaders, and external partners on clinical studiesQUALIFICATIONS & EXPERIENCE:Preferred Bachelor’s degree with 8+ years’ of industry experience, Master’s degree with 6+ years’ of industry experience, PhD with 3+ years’ of industry experienceExperience in managing clinical studies in all phasesExperience with compound lifecycle from IND to NDAThorough understanding of FDA, EMEA, and ROW ICH and GCP guidelines, as well as thorough understanding of cross-functional clinical processes including and not limited to data management, biostatistics, medical monitoring, drug safety, and regulatory affairsExperience with regulatory compliance audits and inspectionsExperience directing and leading in a complex team environment#LI-RemoteVir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology SAN FRANCISCO, CA
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking a candidate with a proven ability to work collaboratively within a matrix environment to support vendor outsourcing activities for Translational and Clinical Development (TCD). They will partner closely with the Head of Development Business Operations to implement new or improved processes, tools and strategies to enable effective outsourcing of services to vendor partners.RESPONSIBILITIES AND LEARNING OPPORTUNITIESDeveloping and maintaining the standards, processes and tools utilized by Development Vendor Outsourcing. Leading the vendor selection lifecycle including Request-for-Information (RFI) and/or Request-for-Proposal (RFP) activities for clinical services such as study management (CRO services), central laboratory, bioanalytical services, interactive response technology (IRT), etc. Contract lifecycle management (drafting, negotiating, executing, tracking, archiving) of vendor agreements including budget and payment terms in accordance to Vir standards and processes. Loading contract financial terms into a structured format to enable efficient review and comparisons of proposals, negotiation of scope and to enable future-state analytics / reporting. Defining and measuring outcome-based key performance indicators (KPIs) for critical service categories. Developing and maintaining strategic partnerships with key vendors to enable effective collaboration and issue resolution. Supporting the budget forecasting activities and quarterly financial reviews with Development Benchmarking & Pricing, Clinical Operations and Corporate Finance. Proactively identifying, defining and implementing new or improved Departmental processes or standardsLeading and managing the Outsourcing team. QUALIFICATIONS AND EXPERIENCE15+ years of relevant clinical development experience preferred with a B.A./B.S. degree; or 10+ years of relevant clinical development experience preferred with an advanced degree.  Ability to utilize complex Microsoft Excel formulas and functions – e.g. VLOOKUP, INDEX, MATCH and pivots. Experience with writing macros or other programming languages a plus. Vir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology SAN FRANCISCO, CA
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking a Senior Director of Biostatistics to provide leadership and oversight to the biostatistics function. This position will report to the head of biometrics.RESPONSIBILITIES AND LEARNING OPPORTUNITIES:Provide biostatistics representation and leadershipLead all aspects of statistical methodology development and implementation.Coordinate with data management and statistical programming to standardize workflow, process, and interaction procedure within Biometrics departmentCollaborate closely with other functions including Clinical Research, Development Operation, Medical Affairs, Regulatory and Research in the appropriate interpretation and effective communication of clinical or other data analysesQUALIFICATIONS AND EXPERIENCE:Ability to work across multiple clinical development programs at the same time and appropriate assess importance, priority, and urgencyExcellent knowledge of recent development of statistical methodology and statistical guideline in pharmaceutical industryStrong leadership and interpersonal skills, especially experience effectively communicating statistics related issues, statistical methods, and statistical analysis results to non-statisticiansExperience of US New Drug Application (NDA), Biologics License Application (BLA), or EU Market Authorization Application (MAA)3+ years of team management experience preferredSuccessful experience in recruiting, mentoring, and developing talented biostatistics team membersEDUCATION:PhD in statistics, biostatistics, or other closely related discipline with 10 + years of prior statistics/biostatistics/biometrics experience in drug-development environment preferredVir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology SAN FRANCISCO, CA
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking an Associate Director of Statistical Programming to own the statistical programming activities to support one or more programs in our clinical development portfolio.RESPONSIBILITIES AND LEARNING OPPORTUNITIES:Provide technical and project management leadership in statistical programming activities to support clinical studies. Accountable for study-level and submission-level statistical programming results on assigned projects, including timelines and quality of deliverables.Interact with statisticians, clinical data managers, clinical trial project managers, medical monitors and other personnel to provide programming support for clinical studies and ad hoc analyses.Review and comment on statistical analyses plans and TFL specifications.Review and comment on CRFs, annotated CRFs, edit checks and related documents.Develop or validate SDTM domain specifications and programs to generate CDISC-compliant SDTM datasets.Develop or validate programming specifications and programs to generate analysis datasets using ADaM standards or study-specific/submission-specific requirements.Develop or validate programs to generate tables, listing and figures based on statistical analysis plan or adhoc requests.Develop and contribute to Biometrics SOPs and working documents related to clinical studies, FDA requests, independent validation, and general statistical programming process.Participate in study team meetings and address issues that may affect statistical programming.Support and participate in the preparation of clinical study report, regulatory submission and annual DSUR safety report.Lead all aspects CRO statistical programming activities and validate their work.Develop and maintain general system macros to facilitate statistical reporting.QUALIFICATIONS AND EXPERIENCE:Excellent verbal and written communication skills and interpersonal skills are required.Strong statistical programming skills using SAS, R and other relevant software.Has a detailed understanding of clinical trial design and reporting process, as well as regulatory reporting requirement in the eCTD format.Ability to read protocols, explore clinical database and make sophisticated judgement about the meaning of, and the patterns in, data.Must be able to interact with others to define and produce user-defined statistical reports (e.g., ad hoc requests).Has the ability to resolve study related issues and conflicts within a therapeutic project.Experience in BLA, NDA/sNDA and EMA submission.EDUCATION:PhD and 7+ years relevant industry experience preferredM.S and 8+ years relevant industry experience preferredB.S and 12+ years relevant industry experience preferredVir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking an experienced Associate Director, Clinical Data Management to join our Clinical Development team. This person will be reporting to the Director, Clinical Data Management and will be providing support to clinical data management activities across one or more clinical development programs enabling planning, coordination, and timely delivery of complete, high quality and reliable clinical trial data for internal decision making, regulatory approval and marketing acceptance.RESPONSIBILITIES AND LEARNING OPPORTUNITIES:Lead and manage CRO in all data management activities for multiple clinical development programs across different stages/phases of development.Serve as the functional representative on project teams and strategic partnerships by providing data management timelines to coordinate and synchronize deliverables with the overall study timelines. Monitor progress and conduct of the study projects, including data cleaning and QC activities to ensure all deliverables are on target with project timelines.Proactively assess risks and develop solutions to complex problems.Lead continuous improvement activities including development of SOPs, standard methodologies, and initiatives within clinical data management.Contribute to project resource planning, vendor evaluation and selection, development of outsourcing strategies and relationships with vendors and partners.Participate in inspection readiness, quality compliance, and training initiatives related to Clinical Data Management.Assist in building and developing team of high performing clinical data managers.QUALIFICATIONS AND EXPERIENCE:Bachelor’s degree: 10+ years of relevant industry experience in Clinical Data Management preferredExperience in providing sponsor oversight for study vendors to ensure completeness, correctness and consistency of clinical data and data structures across programs.Strong knowledge of project management principles and ability to manage multiple competing tasks and fast changing priorities.Advanced knowledge and experience of Data Management processes and systems.Strong knowledge and understanding of industry standards including ICH, GCP, CDASH/CDISC and other applicable guidelines.Experience with regulatory submission requirements [e.g., New Drug Application (NDA)/Biologics License Application (BLA)/Market Authorization Application (MAA)].Vir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking an experienced computational structural biologist/molecular modeler to join the structural biology group. The successful candidate will be responsible for developing and utilizing a structure- and sequence-based protein engineering platform to support Vir's drug discovery efforts.RESPONSIBILITIES AND LEARNING OPPORTUNITIESPlan, develop, and employ a computational modeling/simulation platform to study protein structure and dynamics, antibody-antigen and other protein-protein interactions, as well as protein-small molecule interactionsDesign and test mutagenesis libraries to guide protein engineering and small molecule design effortsDetermine, analyze, and predict epitopes and paratopesDevelop a repository database for routine analysis, visualization, and storage of protein structure and engineering dataWork with Vir’s Data Sciences department to employ additional computational tools, (such as bioinformatics, machine learning) to augment modeling outcomes Identify the most relevant methods and techniques for each purpose, and optimize them by systematically exploring relevant parametersManage external partners/collaborations, as necessaryQUALIFICATIONS AND EXPERIENCEBS/BA and 12+ years, MS and 10+ Years or PhD and 5+ years of relevant experience in computational chemistry, molecular modeling, structural biology, or related field preferredDemonstrated track record of successfully applying computational structural biology and protein engineering methods to solve scientific problems relevant to drug discoveryDeep understanding of the antibody discovery process from initial hit to lead selectionExpert knowledge of modern computational chemistry packages and tools, with an emphasis on molecular dynamics, structure prediction and analysis, virtual screening/docking, and free energy determinationExpert knowledge of relevant programming/scripting tools, such as Python, Bash, CUDAPublications in peer-reviewed scientific journals.Vir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Job Summary:Vir is seeking a Senior Scientist of Bioanalytics who will be responsible for developing bioanalytical methods to support development of large molecule assets. This individual will oversee the development, execution, and reporting of bioanalytical analyses, including contribution to regulatory documents, and will work cross functionally to ensure reliable data are provided to end-users in accordance to GXP requirements. The candidate will be responsible for the management of external vendors, participate in vendor audits, and be responsible for managing all aspects of method development, validation, study sample analysis, and reporting of data. (Small molecule expertise is a plus).RESPONSIBILITIES AND LEARNING OPPORTUNITIES:Responsible for developing bioanalytical methods to support large and small molecule clinical candidates and providing bioanalytical input across all functional areas and stages of research and development.Responsible for coordinating method development and analysis activities within the context of development plans.Performs troubleshooting and evaluation of a variety of complex methods in order to identify appropriate bioanalytical solutions.Responsible for leading technology transfer of bioanalytical methods, as appropriate.Responsible for interacting with internal Research, CMC, Operational, and Regulatory groups to support drug development activities.Responsible for review and approval of data and reports from external vendors.QUALIFICATIONS AND EXPERIENCE:PhD with 5+ years /MS and 8+ years/BS and 10+ years of industry experience preferred.Experience must include a combination of laboratory and project management skills, including managing CROs for assay development and validation for clinical and non-clinical studies. Demonstrated expertise in GLP and GCP compliance of sample handling and storage, bioanalytical assay development, sample analysis, and laboratory operation and procedures/processes is required. Technical expertise with a wide variety of platforms to analyze all aspects of large molecule therapeutics, including those with complex sample handling and preparation procedures (e.g., enzymatic assays, ligand-binding assays, cell-based assays, etc.) from a variety of biological matrices (e.g., serum, plasma, etc.). Small molecules expertise is a plus.Familiar with PK and PD principles pertaining to establishment of relevant assays and assay ranges.#LI-RemoteVir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Job Summary:Vir Biotechnology is seeking a Clinical Pharmacologist to support of all phases of drug development for from early clinical development, market application, and commercialization.RESPONSIBILITIES AND LEARNING OPPORTUNITIES:The candidate is responsible for clinical PK and/or PK/PD study design, analysis, interpretation, operation, and reporting to support clinical development and international regulatory submissions (e.g., clinical protocols and reports, IB, IND, NDA/BLA). This candidate will have broad responsibilities within the department designing, operationalizing, and analyzing data from clinical studies that evaluate the ADME, safety, and/or efficacy of drug candidates.Additional responsibilities include presenting clinical pharmacology data, acting as a technical expert on cross-functional project sub-team and/or project sub-teams.Understanding and ability to guide quantitative/modeling efforts. Hands-on experience with Population PK modeling and/or PBPK, PK/PD modeling.QUALIFICATIONS AND EXPERIENCE:PhD with 5+ years /MS and 8+ years/BS and 10+ years of industry experience preferred.PhD, PharmD, or MD with relevant training in Clinical Pharmacology, pharmacokinetics, pharmaceutics, or related field with 3+ years of experience working in Clinical Pharmacology preferred.Familiarity with the drug development process and the role of Clinical Pharmacology. Candidate with experience in designing and facilitating operation and reporting of various Phase 1 studies and Phase 2/3 studies with respect to dose selection/justification, advanced analysis of demographic and disease characteristics (i.e., PK/PD) is preferred.Ability to translate preclinical data into clinical dosing schemes, including projection of PK in humans. Experience independently developing and/or guiding development of PK and PK/PD models. Must be operational on analysis and graphing software (e.g., SAS, R, Phoenix WNL, GraphPad, etc).  #LI-RemoteVir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology SAN FRANCISCO, CA
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking an experienced cell biologist to join our molecular pharmacology team working on the discovery of small molecules as immunomodulators for the treatment of infectious diseases. This includes target validation, generation and optimization of biophysical, biochemical and cellular assays, as well as cellular pharmacology assays to test the activity of compounds on the target biochemical pathway in a natural cellular environment.The team’s success is based on a collaborative and supportive atmosphere and on sharing of expertise of team members in different specialties. This creates outstanding professional development opportunities even for experienced individuals, an enjoyable working environment and above average chances of success for our projects. RESPONSIBILITIES & LEARNING OPPORTUNITIES:Generation and maintenance of transiently transfected cells, stable cell lines and primary cells Design and generation of expression vectors and transfection of target cellsEstablishing biochemical and cellular assays including optimization and QCTesting of compounds in various assays to characterize their activity and molecular mechanism of actionData recording, analysis and presentation at group meetings.QUALIFICATIONS & EXPERIENCE:Preferred Bachelor’s degree in biology/biotechnology or related discipline, 4-5 years of industry experience; Master’s degree with 2-3 years of industry experience preferredSolid hands on experience in molecular biology and cell culture including cell line generation. Good trouble shooting skills.Understanding of cellular biology and basic concepts of pharmacology, ideally with experience on cells of the innate immune system.Experience with lab automation is a plusThe candidate should enjoy working in a team and share problems and solutions as integral part of the work routine. Vir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology SAN FRANCISCO, CA
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking a committed scientist with a track record of results to work both collaboratively and independently to help drive progress in our drug discovery pipeline. Primary focus on advancing early-stage host targets relevant to infectious disease via mechanism of action studies particularly in the natural cellular environment, pharmacological validation, and iterative optimization of small molecules, encompassing diverse methods as appropriate for each project. This position requires strong adaptability, experimental savvy, and the drive to deliver high quality results in a timely manner. The team’s success is based on a collaborative and supportive atmosphere and on sharing of expertise of team members in different specialties. This creates outstanding professional development opportunities as well as an enjoyable working environment.RESPONSIBILITIES & LEARNING OPPORTUNITIES:Assesses the experimental need and generates plan to address the need in close consultation with other team members.Establishes and performs mechanistic studies and cellular and biochemical assays.Analyzes results, documents experiments, and presents work in multiple forums including 1-on-1, in departmental or cross-functional project team meetings, and in cross-Research seminars.Adapts to and thrives in a dynamic environment with evolving priorities/needs and a wide-ranging portfolio.Efficiently manages work that over time will likely span multiple projects, and thus prioritizes efforts in order to deliver high quality results in a timely manner.Over time, contributes to project planning and identification of research opportunities.QUALIFICATIONS & EXPERIENCE:Preferred qualifications of bachelor’s degree in biology or related discipline with 8+ years industry experience; OR Master’s degree with 6+ years industry experience; OR PhD without industry experienceStrong track record of delivering results, particularly at the bench. A strong record of publications and/or internal promotions, for example, would be considered a major plus. Experience in the following areas is a plus: cell culture, infectious diseases, cell and molecular biology, microscopy, biochemical assays, liquid handling and automation, high throughput screening.The candidate should enjoy working in a team and share problems and solutions as integral part of the work routine.Vir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology SAN FRANCISCO, CA
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Bio is seeking an experienced bioinformatics engineer who will work with the Data Science team in San Diego or in San Francisco (potential for remote work) to develop robust, high-performance pipelines that can accurately and optimally manage and analyze a diverse set of sequencing and experimental data. A key focus for the bioinformatics engineer is to bring data and analytical capabilities forward from concept, through feasibility, and into production in cloud environments. The Data Science team, formed by engineers, bioinformaticians, genome analysts and machine learning specialists, builds data infrastructure, pipelines and data analytics across the company.RESPONSIBILITIES AND LEARNING OPPORTUNITIES:Collaborate with data scientists, software engineers, and with scientists in wet labs to derive insights from large-scale data sets.Develop and maintain clean, reusable, composable, and scalable bioinformatics and data pipelines.Establish best practices for development, testing, and optimization of bioinformatics workflows.Review, extract, and transform data and lead all aspects of data quality and data access constraintsContribute to the data infrastructure at Vir: databases, APIs, scripts, and applications.QUALIFICATIONS AND EXPERIENCE:5+ years’ experience in a relevant bioinformatics role preferred.Proven track record of developing and deploying computational pipelines in cloud-based environments using tools such as Docker and/or Kubernetes. Familiarity with pipeline/workflow languages such as Nextflow or WDL a plus.Expertise and experience with AWS technologies including S3, RDBS, Batch, Lambda, Athena a plus.Extensive experience analyzing NGS data and familiarity with standard tools such as BWA, samtools, GATK, STAR, etc.Practical experience with pathogen sequencing and single-cell data sets a plus.At least 5 years’ experience programming in Python (and/or R) for method development and data analysis.Collaborative code development as part of a team a plus.Fundamental knowledge about database technologies and strong SQL skillsClinical data management expertise and experience working with sensitive data a plus.Demonstrated commitment to software development best practices, including version control (git or similar), unit testing, continuous integration, issue tracking, software life cycle and code sharing.Strong written and verbal communication skills, with an ability to communicate effectively with both scientific and engineering groups.Ability to lead multiple simultaneous projects and bring projects to a successful, timely completion.EDUCATION:Bachelor's, Master’s Degree or PhD in Bioinformatics, Computational Biology, Computer Sciences or related area; and/or equivalent experience/training.Vir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking an experienced and highly motivated scientist to join our Clinical Virology team in a leadership role, focused on managing pre-clinical research and clinical development of novel therapies for infectious diseases. The successful candidate will independently lead clinical virology activities for a therapeutic area, including management of virology activities for clinical trials, characterization of viral resistance, and lead pharmacology contributions for regulatory submissions. This role will work cross-functionally across research and development groups within the company to advance programs through clinical development.RESPONSIBILITIES AND LEARNING OPPORTUNITIES:Independently lead clinical virology activities to support clinical trials, from study start up through study report delivery, including representing virology in study management and clinical sub teamsManage external contract research labs to support clinical virology deliverables, including working cross functionally to meet timelines and budgets for clinical virology assays.Author clinical virology reports and section of key clinical and regulatory documents.Oversee pre-clinical and clinical scientific research internally or at contract labsInvestigate the feasibility of applying a wide variety of scientific principles and concepts and/or development strategies in research and development.Lead non-clinical pharmacology data packages for regulatory submissions, including authoring and review of IND documentsProvide updates to management teams on status of pre-clinical and clinical virology activities. Stakeholder management with internal business partners, key opinion leaders, and external partners on clinical studiesQUALIFICATIONS AND EXPERIENCE:PhD with 7+ years of relevant experience or equivalent degree/experience in microbiology, virology, or a related field preferred. Experience supporting clinical trials and/or working with clinical samples requiredBackground in respiratory viruses and/or chronic viral diseases highly desirablePrior experience managing teams, including managing scientists, contract labs or working across companiesProficiency in cell-based virology and molecular biology techniques, including assay development. Experience in qPCR, cell-based viral quantification, viral sequencing, and/or viral resistance is highly desirable. Excellent written and verbal communication skills and strong project management/organizational skills are essential.#LI-Remote Vir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.
Vir Biotechnology SAN FRANCISCO, CA
Vir is a clinical-stage immunology company with a compelling mission: “A World Without Infectious Disease”. We are focused on combining immunologic insights with cutting-edge technologies. We have assembled four technology platforms that are designed to stimulate and enhance the immune system by exploiting critical observations of natural immune processes. Our current development pipeline consists of product candidates targeting COVID-19, hepatitis B virus, influenza A and human immunodeficiency virus. We believe the success of our colleagues drives the success of our Mission. We have an ongoing commitment to creating a company passionate about equality, inclusion, and respect. When everyone feels supported and encouraged to give at their best, we will collectively deliver outstanding results. Vir Biotechnology is seeking a highly talented and motivated Research Associate II to join our Clinical Immunology team. The successful candidate will help drive new efforts in the discovery and development of novel therapies for the treatment of infectious diseases including HIV, HBV, SARS-CoV-2 and others. You will work within a highly collaborative group, participating in discovery and translational research efforts aimed at identifying and characterizing novel therapeutic targets, and investigating mechanism of action of therapeutics.RESPONSIBILITIES AND LEARNING OPPORTUNITIES:Work under the supervision of scientists to conduct scientific research that furthers our understanding of the human immune response to infectious diseases and therapeutic interventions.Responsible for the optimization, execution, and analysis of complex immunologic assays.Assist with primary cell isolation.Document accurate records of experimental details and results related to assigned projects.Maintain project timelines and actively participates in team meetingsAssists in ordering supplies, making reagents, and maintaining the laboratory to conduct necessary activities.Actively seeks opportunities to continuously improve and learn.QUALIFICATIONS AND EXPERIENCE: BS/BA with preferred 2 plus years of experience OR MA/MS/MBA with no experience ideally in biological sciences or related field with 2+ years of lab experience (background in immunology and infectious disease research preferred).Demonstrated track record of productivity with flow cytometry, antibody-based assays, and cell culture aseptic technique.Hands-on experience in a wide variety of cell biology & molecular biology techniques, including isolation of immune cells from peripheral blood or apheresis materials.Detail oriented with the ability to work independently and manage multiple competing priorities in a fast-paced team environment.Professional interpersonal skills, excellent oral/written communication skills.Proficiency in Microsoft Office applications is requiredHighly desirable: experience with optimizing various immunological assays (T cell stimulation assays, 8+ color flow cytometry, ELISA, RNAseq, etc), and data analysis software/programs (FlowJo, SPADE, SPICE, Cytobank, Prism, Spotfire, R, etc.)Vir’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 benefits and perks such as: health, dental, vision, life and disability insurance benefits, non-accrual paid time off, one Friday a month paid-time off, company shut down for holidays, commuter benefits, child care reimbursement, education reimbursement, 401K match and lunch for all lab essential personnel!Vir is an equal opportunity employer.  We value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform critical job functions, and to receive other benefits and privileges of employment. Please contact Human Resources to request accommodation.Vir Human Resources leads recruitment and employment for Vir. Unsolicited resumes sent to Vir from recruiters do not constitute any type of relationship between the recruiter and Vir and do not obligate Vir 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.