JOIN US IN THE FIGHT AGAINST CANCER

BeiGene continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

OpeningsLocationJob SummaryDepartmentDetail
IT Senior Business Analyst, Enterprise ApplicationsCambridge, New Jersey, San Mateo and EmeryvilleAs a member of BeiGene’s Global Enterprise Applications team, the purpose of this role is to plan, design, configure, support and deploy all GxP and G&A systems including HRIS, CLM, CTMS, Clinical, Biometrics, Quality and other enterprise business systems in support of core organizational functions and processes primarily in the Cloud/SaaS, Amazon Web Services (AWS) and Azure environments.Information TechnologyDetail
IT Manager of Enterprise ApplicationsCambridge, MA, San Mateo, CA or Emeryville, CA, or Fort Lee, NJAs part of BeiGene’s Global Enterprise Applications team, the IT Manager of Enterprise Applications will be responsible for implementation and management of BeiGene’s enterprise applications to meet regulatory requirements and business needs.Information TechnologyDetail
PARALEGALCambridge, MABeiGene’s first Paralegal will join and support the diverse needs of our experienced and dynamic in-house legal team, primarily in the area of corporate governance. The Paralegal will also assist with other legal responsibilities and initiatives at BeiGene, including invoice administration and litigation, privacy and security support.LegalDetail
CONTRACTS ADMINISTRATORCambridge, MA, San Mateo, CA or Emeryville, CABeiGene’s first Contracts Administrator will be a key member of the Legal team. Under the supervision of the Sr. Director, Legal Operations, they will work closely with business partners throughout the company to ensure the appropriate organization and maintenance of BeiGene contracts and records.LegalDetail
Sr. Network Engineer, IT OperationsEmeryville, CA or San Mateo, CA the Sr. Network Engineer will support the Global IT network infrastructure. The candidate will be an instrumental part of IT team in implementing the IT vision and enhancing BeiGene’s current systems, process and infrastructure necessary to support future growth and expansion plans.Information TechnologyDetail
MANAGER/SR MANAGER, REGULATORY AFFAIRSSan Mateo or Emeryville CAThe Manager/Senior Manager, Regulatory Affairs will manage, evaluate, and complete regulatory projects consistent with company goals. This individual will be responsible for timely planning and coordination of regulatory submissions and provide guidance to cross-functional teams on regulatory strategy and tactics.Regulatory AffairsDetail
ASSOCIATE/SENIOR ASSOCIATE IN REGULATORY
San Mateo or Emeryville CAThis individual will be responsible for timely planning and coordination of regulatory submissions and provide guidance to cross-functional teams on regulatory strategy and tactics.Regulatory AffairsDetail
DIRECTOR, REGULATORY AFFAIRSSan Mateo or Emeryville CAThe Director, Regulatory Affairs will be responsible for developing, implementing, and advising on global regulatory strategies for development programs to secure and maintain market access for product(s) in line with business objectives, and in coordination with key internal stakeholders.Regulatory AffairsDetail
ReceptionistCambridge, MAThe Receptionist is part of the Administrative Support Team; a team whose functional role is to provide a wide variety of support services to the entire organization. AdministrativeDetail
Senior Manager, HRISEmeryville or San Mateo, CABeiGene is hiring a Senior Manager, HRIS who will be responsible for the development and management of the HRIS platform, including implementation, integration, and configuration.Human ResourcesDetail
Contracts ManagerCambridge, San Mateo, CA or Emeryville, CA.We are seeking a non-attorney contracts specialist to complement our growing internal Legal Department as we further our vision to develop and commercialize molecularly targeted and immuno-oncology cancer therapeutics. This individual will be instrumental in supporting the contracting needs of our many different functions, by serving as one of the legal contacts for contracting matters.LegalDetail
SENIOR MANAGER, HRBPCambridge, MA or Fort Lee, NJSenior Manager HRBP is responsible for translating business objectives into organizational and talent strategies. Working with senior executives, managers, and employees in the areas of G&A, Finance, Legal, Clinical Operations, and Biometrics, this role will focus on complex organizational development opportunities and building leadership capability at all levels.Human ResourcesDetail
Senior Director, Global Health Economics Research (HEOR)RemoteSenior Director, Global Health Economics Research (HEOR)This individual is accountable for providing direct leadership of the global HEOR arena and matrix leadership to executives across Immuno-Oncology & Hematology. Medical AffairsDetail
Senior Manager, Clinical Outsourcing, RemoteRemoteThis position will be responsible for the coordination and management of strategic clinical sourcing needs in support of BeiGene’s current and planned clinical trials (global or in the Asia Pacific region, particularly in China and Australia), including vendor identification and selection, Request for Proposal (RFP) and Bid Defenses, negotiating contracts, managing outsourcing budgets, vendor performance metrics, and vendor oversight/governance.Clinical OutsourcingDetail
Senior Benefits ManagerEmeryville or San Mateo, CAThe Benefit Manager’s primary responsibility includes managing the entire scope of employee benefits including but not limited to fringe benefits, cafeteria plans, leave of absences, wellness initiatives, benefit compliance, claims resolution, and open enrollment initiativesHuman Resources Detail
Senior Manager / Associate Director, Investor RelationsCambridge MASenior Manager / Associated Director of IR will report to the Head of IR and will help develop and execute the organization’s IR strategy. Responsibility will include strategic positioning of the corporate message, interfacing with the investment community, identifying / targeting global investor groups, and developing investor materials and Q&A.Finance and StrategyDetail
Executive Assistant/Senior Administrative AssistantSan Mateo, CAThe person in this role will need to be an experienced problem-solver with exceptional flexibility to work across multiple disciplines across our clinical trials.Program ManagementDetail
Senior Manager or Associate Director, Inspection ManagementSan Mateo, Emeryville CAThe Senior Manager or Associate Director of Inspection Management will be based in San Mateo or Emeryville, CA. This will be a hands-on position that will be responsible for the organization, planning, process and logistics of all health authority inspections. Quality AssuranceDetail
Sr. Manager / Associate Director, GMP QAEmeryville CA, San Mateo CAThe incumbent is responsible for overseeing quality operational activities and programs related to GMP Quality. Develops, interprets, and implements quality policies and supports regulatory compliance inspections.QualityDetail
Senior Manager/ Associate Director, Quality Systems DevelopmentEmeryville or San Mateo, CAThe position's primary purpose is to manage the implementation and improvement of Quality Systems, Quality processes, and refine Quality project management methodology.Quality AssuranceDetail
Manager/Sr Manager, Clinical Systems Validation QASan Mateo or Emeryville, CAManager/Sr. Manager of Computer Systems Validation QA will oversee the GxP computerized systems validation and provide QA oversight within BeiGene.QualityDetail
Drug Safety Scientist/Senior ManagerSan Mateo or Emeryville, CAThe person in this position collects, analyzes and displays safety data to allow medical interpretation and action concerning potential and actual safety signals with assigned products. This person will assist more senior staff in creating reports and archiving documentsDrug SafetyDetail
Director, Supply Chain & Logistics - Commercial PlanningEmeryville, San Mateo, CA and Cambridge MAThe Director of Commercial Planning manages drug supply activities related to Finished Good demand planning for launch and commercial products.Supply Chain & LogisticsDetail
Manager, Clinical Supply Chain and LogisticsEmeryville, San Mateo, CA and Cambridge MAThe Manager of Clinical Supply Chain and Logistics manages drug supply activities related to planning, label development, label & pack, and distribution for several clinical studies.Clinical Supply Chain and LogisticsDetail
Associate Director, Clinical Supply Chain and LogisticsEmeryville, San Mateo, CA and Cambridge MAThe Associate Director of Clinical Supply Chain manages drug supply activities related to planning, label development, label & pack, and distribution for one or more clinical programs.Clinical Supply Chain and LogisticsDetail
Manager/Senior Manager of StrategyCambridge, MAThe position is based in Cambridge, MA. Manager/Senior Manager of Strategy participates in BeiGene’s business analytics and financial planning efforts by providing objective and in-depth analyses of current and future pharmaceutical markets, including product performance, market access landscape, and impact of regulatory policy updates.Finance and StrategyDetail
Senior Clinical Investigator Contract & Budget AssociateEmeryville or San Mateo CAThe Investigator Contract & Budget Associate, reporting to the Investigator Contract & Budget Manager, is responsible for the development and analysis of contractual relationships including investigator grants including but not limited to drafting, negotiating, and finalizing agreements related to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations.Investigator Contract Management (ICM)Detail
Senior Manager, Statistical ProgrammingNJ/Cambridge, MA/Emeryville CA/San Mateo CAThe Senior Manager, Statistical Programming will work in BeiGene's Statistical Programming group to manage and support Statistical Programming deliverables for multiple clinical studies.Biostats/Statistical ProgrammingDetail
Senior Manager/Associate Director of GCP Quality AssuranceSan Mateo or Emeryville CAThe Associate Director, Clinical Quality Assurance is responsible for implementing and maintaining a balanced, proactive, and phase appropriate approach to GCP Quality Assurance.Quality AssuranceDetail
Director, GMP QA, Oral Solid Dosage (OSD)San Mateo or Emeryville CAThe Director, GMP QA OSDOSD is responsible for overseeing quality operational activities and programs related to OSD manufacturing.QualityDetail
Associate Manager, Clinical OperationsSan Mateo or Emeryville CA or Cambridge MALeads some aspects of assigned clinical trial(s) and demonstrates a good level of knowledge of clinical operations�methodologies, organizational, project management and leadership capabilitiesGlobal Clinical OperationsDetail
Senior Manager, Statistical ProgrammingNJ/Cambridge, MA/Emeryville CA/San Mateo CA

The Senior Manager, Statistical Programming will work in BeiGene’s Statistical Programming group to manage and support Statistical Programming deliverables for multiple clinical studies.BiometricsDetail
Manager, Statistical ProgrammingEmeryville CA, San Mateo CAThe Statistical Programming Manager will work in BeiGene's Statistical Programming group. The position is an individual contributor role and will primarily involve project management of clinical studies in Phase I-IV.Statistical ProgrammingDetail
Manager/Senior Manager, Global New Product PlanningCambridge, MAReporting to the Director of New Product Planning, this position is responsible for developing commercial perspectives for pipeline assets, building revenue forecast and managing product launch preparation projects. Finance, Investor RelationsDetail
Senior Biomarker Operations AssociateEmeryville or San Mateo CAThe Senior Biomarker Operations Associate will support BeiGene’s early and late stage pipeline programs by the successful execution of deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners.Detail
Clinical Investigator Contract & Budget ManagerEmeryville or San Mateo CAThe Contract & Budget Manager will undertake activities to provide specialized support and manage the investigator contract lifecycle process and manage staff within the well as support other Departments, as required, which are involved in the planning, execution, management Investigator Contract Management Office as and tracking of global clinical trials which may be subcontracted to an external service providerInvestigator Contract Management (ICM)Detail
Director, BiostatisticsEmeryville or San Mateo, CASupporting the BTK-3111 clinical development with a focus on hematology area, the position will work with the clinical and regulatory team in designing clinical trials and developing the statistical analysis plan, facilitate the implementation of statistical analyses, provide statistical input to the CSR and scientific presentations/manuscripts, perform statistical functions for submission related activities and serve as internal statistical expert in the overall program. BiostatisticsDetail
Associate Director, BiostatisticsEmeryville or San Mateo, CASupporting the BTK-3111 clinical development with a focus on hematology area, the position will work with the clinical and regulatory team in designing clinical trials and developing the statistical analysis plan, facilitate the implementation of statistical analyses, provide statistical input to the CSR and scientific presentations/manuscripts, perform statistical functions for submission related activities and serve as internal statistical expert in the overall program. BiostatisticsDetail
Associate Director, Statistical Programming Beijing/ Shanghai,ChinaThe Assoc. Director, Statistical Programming will work in BeiGene¨¹s Statistical Programming group to manage and support Statistical Programming deliverables for multiple clinical studies.BiometricsDetail
Mgr, Statistical Programming Beijing/ Shanghai,ChinaThe Statistical Programming Manager will work in BeiGene¨¹s Statistical Programming group. The position is an individual contributor role and will primarily involve project management of clinical studies in Phase I-IV.BiometricsDetail
Sr Mgr, Statistical Programming Beijing/ Shanghai,ChinaThe Senior Manager, Statistical Programming will work in BeiGene¨¹s Statistical Programming group to manage and support Statistical Programming deliverables for multiple clinical studies.BiometricsDetail
Medical director, Clinical development Beijing/ Shanghai,ChinaProvide overall medical and safety oversight and monitoring of outsourced or in-house oncology clinical studiesClinical DevelopmentDetail
Director or AD, Clinical Monitoring Beijing/ Shanghai,ChinaDirector of Clinical Monitoring, Clinical Operation is accountable for the overall delivery of the responsible teamClinical OperationDetail
Manager, Clinical Monitoring Beijing/ Shanghai,ChinaManager of Clinical Monitoring, Clinical Operation is accountable for the delivery of the responsible teamClinical OperationDetail
Manager, Clinical Operations Beijing/ Shanghai,ChinaClinical Operation Manager is accountable for trial delivery with high quality, and within timeline and budgetClinical OperationDetail
Associate Director / Director, Clinical Budget Planning and Analysis Beijing/ Shanghai,ChinaAccountable for Clinical Budget Planning, tracking and Analysis for trials led by China COMsClinical OperationDetail
Associate Manager, Clinical Operations Beijing/ Shanghai,ChinaMonitor and manage clinical trial according to ICH/GCPClinical OperationDetail
Director or Associate Director, Clinical Start Up Beijing/ Shanghai,ChinaAccountable for the study start-up timelines and delivery, with high quality and according to ICH/GCPClinical OperationDetail
Manager, Clinical Start Up Beijing/ Shanghai,ChinaLead Startup specialist to the delivery of clinical start-up component of assigned studies with accountability for time, cost and quality for assigned activitiesClinical OperationDetail
Medical Science Liaison Beijing/ Shanghai,ChinaMedical AffairsDetail
Specialist, Clinical Start Up Beijing/ Shanghai,ChinaAccountable for the study start-up timelines and delivery, with high quality and according to ICH/GCPClinical OperationDetail
CTA Beijing/ Shanghai,ChinaClinical OperationDetail
Asia-Pacific Regional Head,Pharmacovigilance and Drug SafetyBeijing, ChinaThe Regional Head will be responsible for the line management of PV personnel in the region who have both local and global roles. The Regional Head will be the PV regulatory expert for the region and the chief PV contact person for the regulatory authorities in the region for investigational and marketed products.PVDetail
Lead, Safety Operations Asia PacificBeijing, ChinaManages the Safety Operations staff of Asia Pacific region including safety operations in support of marketed products managed through the Shanghai office. Provides regional support for all ICSR management and associated internal and external queries in close coordination with global safety operations.PVDetail
Affiliate PV ManagerShanghai, ChinaProvide PV services to local affiliate in fulfillment of SDEA with partner including local adverse event collection and follow up as needed, recxonciliation with partner database and support of other post-approval PV commitments.PVDetail
Research investigator/ Senior research investigator Preclinical tumor ImmunologyBeijing, Chinadesign and execute proof of concept studies in pre-clinical models of tumor immunology, and assist in cross-functional development of our research strategy.ResearchDetail
QA Specialist/ SupervisorBeijing, ChinaInitiate QA SOPs and coordinate the initiation, review and approval of SOPs and documents.ResearchDetail
Senior Scientist in Biologics- Antibody generationBeijing, ChinaDesign and arrange experiments independently
ResearchDetail
Senior Manager, BiostatisticsEmeryville, CA; San Mateo, CASupporting the BTK-3111 clinical development with a focus on hematology area, the position will provide high quality statistical support to assigned projects/studies with support of senior staff as necessary.BIOSTATISTICSDetail
MANAGER, IRT VALIDATIONCambridge, MAThe primary responsibility of the Manager, IRT Validation is to manage BeiGene¨¹s companywide Interactive Response Technology (IRT) processes related to User Acceptance Testing.Global Clinical Development OperationsDetail
Associate Director Cancer GenomicsEmeryville, CA; San Mateo, CAThe Associate Director Cancer Genomics will support BeiGene¨¹s compound development programs by assessing genomic biomarkers and signatures across retrospective and prospective datasets, with the goal of developing novel companion diagnostics as appropriate. Detail
Associate Director/Director Clinical ScienceEmeryville, CA; San Mateo, CAThe Associate Director/Director ¨¹ Clinical Science will support BeiGene Clinical and Medical assets by successful execution of clinical development programs and deliverables in partnership across the organizationDetail
Site Lead, IT OperationsCambridge MAReporting to the Director, IT Operations, the Site Lead, IT Operations will support the day to day IT operations of the Company¨¹s office in Cambridge, MA.Information TechnologyDetail
Senior Clinical Database QA EngineerCambridge MAClinical database QA engineer is responsible for all QA aspects of study build, validation, and maintenance, including QC activities for new and ongoing clinical studies, start-up activities, database revisions, timely resolution of technical issues related to the conduct and closeout of clinical studies.Clinical InformaticsDetail
Senior Clinical Database ProgrammerCambridge MAThe clinical Database Programmer is responsible for all technical aspects of study build, validation, and maintenance, including clinical programming activities for new and ongoing clinical studies, start-up activities, database revisions, timely resolution of technical issues related to the conduct and closeout of clinical studies.Clinical InformaticsDetail
Associate Director, Clinical Supply Chain and LogisticsEmeryville, CA; San Mateo, CAThe Associate Director of Clinical Supply Chain manages drug supply activities related to planning, label development, label & pack, and distribution for one or more clinical programs. Global Clinical Development OperationsDetail
Manager/Senior Manager/Associate Director, Investor Relations and Corporate CommunicationsCambridge MAThe position is based in Cambridge, MA, US. The role will work on investor activity planning, press release drafting and review, and interaction with investment stakeholders to support the company¡¯s financial activities.Finance and StrategyDetail
Executive Director, Safety ScienceEmeryville, CA; San Mateo, CA; Cambridge MAThe Executive Director, Safety Science manages and leads the function in PV and Drug Safety responsible for the identification, characterization and communication of the risks associated with BeiGene products under development and on the market and in concert with other functions developing and communicating risk mitigation strategies both internally and externally to regulators, clinical investigators and patients.Pharmacovigilance and Drug SafetyDetail
Senior Manager, Clinical OperationsEmeryville, CA; San Mateo, CAResponsible for the planning, implementation and conduct of large, global, complex oncology clinical trials in Phase I-IV; or multiple smaller early-phase studies.
Global Clinical OperationsDetail
Assoc. Director, Statistical ProgrammingSan Mateo, CAThe Assoc. Director, Statistical Programming will work in BeiGene¡¯s Statistical Programming group to manage and support Statistical Programming deliverables for multiple clinical studies.BiometricsDetail
Director, Clinical ScienceEmeryville, CA; San Mateo, CAThe Director _ Clinical Science will support BeiGene Clinical and Medical assets by successful execution of clinical development programs and deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners.Global Clinical DevelopmentDetail
Senior Director, Clinical ScienceEmeryville, CA; San Mateo, CAThe Senior Director _ Clinical Science will support BeiGene Clinical and Medical assets by successful execution of clinical development programs and deliverables in partnership across the organization; with external vendors; and with external academicians and collaboration partners.Global Clinical DevelopmentDetail
Senior Medical WriterEmeryville, CAThe Senior Medical Writer is responsible for writing, editing, and formatting clinical regulatory documents that conform to domestic and/or international regulatory submission and internal document standards, while meeting project timelines.Detail
Associate Director, Program ManagementEmeryville, CADevelop project plans with established goals, milestones, timelines, and budget. Partner with function heads, external partners, and the project team to ensure project is on track and aligned with corporate goals.Program ManagementDetail