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
Service Desk Technician IISan Mateo, CAReporting to the Director, IT Operations, System support analyst will assist in support of the day to day IT operations of the Company’s office in Emeryville office. They will support the delivery of technology services that support and improve business processes for the users. Assist in delivery of incident and service request management.Information TechnologyDetail
Clinical Research Associate (CRA)San Mateo, CA or Emeryville, CA or Ft. Lee, NJ or Cambridge, MAThe CRA executes clinical trial protocols at clinical trial sites and monitors clinical trials in accordance to ICH guidelines and GCP, local regulations, and applicable SOPs. Performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Oncology and Pharma clinical trials within the assigned region.Clinical OperationsDetail
Senior Clinical Research Associate (SCRA)San Mateo, CA or Emeryville, CA or Ft. Lee, NJ or Cambridge, MAThe CRA performs monitoring activities related to initiation, conduct (recruitment, quality data collection) and timely completion of Oncology and Pharma clinical trials within the country.

The CRA is responsible to deliver data within timelines and required quality standard, responsible for adherence to monitoring procedures in accordance with GCP and ICH, local regulations and SOPs.
Clinical OperationsDetail
Senior Business AnalystEmeryville, CA, San Mateo, CA, Cambridge, MA or Ridgefield, NJReporting to our Director of IT Enterprise Applications, you will be responsible for the planning, designing, configuration, administration and maintenance of business critical enterprise This is a technical, hands-on role supporting various GxP and G&A systems including HRIS, CLM, CTMS, Clinical, Biometrics, Quality and other enterprise business systems which is primarily Cloud/SaaS based or hosted on-prem on our Amazon Web Services (AWS) IaaS environmentsInformation TechnologyDetail
Manager/Senior Manager, Drug Safety SystemsSan Mateo, CA or Emeryville, CAProvide support for the Argus Safety System and other associated Drug Safety systems and data repositories. Working with the Drug Safety Systems team, this individual will provide technical expertise, support and guidance to the BeiGene PV and Drug Safety Department to facilitate the processing and submission of ICSRs, aggregate safety reports, safety analyses, signal detection, and also respond to time-sensitive requests from internal and external stakeholders such as Drug Safety/PV Scientists, Clinical Science, regulatory authorities and/or business partner ad hoc requests.Drug Safety
IT Manager of Enterprise ApplicationsEmeryville, CAAs 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 the business needs for global G&A functions within BeigeneInformation TechnologyDetail
Manager, ContractsSan Mateo, CA; Emeryville, CA or, Cambridge, MAWe are seeking an experienced 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
Contracts CounselSan Mateo, CA; Emeryville, CA or, Cambridge, MAWe are seeking a dynamic contracts/transactional attorney to complement our growing internal Legal Department as we further our vision to develop and commercialize molecularly targeted and immuno-oncology cancer therapeutics.LegalDetail
Senior Business Analyst, Veeva Center of ExcellenceEmeryville, CA; San Mateo, CA; Cambridge, MA or, Fort Lee, NJAs part of BeiGene’s Global Enterprise Applications team, the Senior Business Analyst, Veeva Center of Excellence, will be responsible for implementation and management of BeiGene’s Veeva application ecosystem to meet regulatory requirements and business needs.Information TechnologyDetail
Biomarker Operations AssociateSan Mateo, CA or Emeryville, CAThe 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. BiomarkersDetail
Senior Field Medical Director - SouthEast Territory SouthEast Territory(Remote)The Senior Field Medical Director (FMD) will support BeiGene Pre-Clinical and Clinical pipeline development by coordinating external collaborations, research endeavors with heath care providers and external academicians while ensuring internal partnership across the organization. Medical AffairsDetail
Senior Field Medical Director - Mid-Atlantic TerritoryMid-Atlantic Territory(Remote)The Senior Field Medical Director (FMD) will support BeiGene Pre-Clinical and Clinical pipeline development by coordinating external collaborations, research endeavors with heath care providers and external academicians while ensuring internal partnership across the organization. Medical AffairsDetail
Senior Field Medical Director - NorthEast TerritoryNorthEast Territory(Remote)The Senior Field Medical Director (FMD) will support BeiGene Pre-Clinical and Clinical pipeline development by coordinating external collaborations, research endeavors with heath care providers and external academicians while ensuring internal partnership across the organization. Medical AffairsDetail
Senior Field Medical Director - SouthWest TerritorySouthWest Territory(Remote)The Senior Field Medical Director (FMD) will support BeiGene Pre-Clinical and Clinical pipeline development by coordinating external collaborations, research endeavors with heath care providers and external academicians while ensuring internal partnership across the organization. Medical AffairsDetail
Senior Field Medical Director - NorthWest TerritoryNorthWest Territory(Remote)The Senior Field Medical Director (FMD) will support BeiGene Pre-Clinical and Clinical pipeline development by coordinating external collaborations, research endeavors with heath care providers and external academicians while ensuring internal partnership across the organization. Medical AffairsDetail
Senior Manager, Learning & DevelopmentEmeryville, CA or San Mateo, CA or Cambridge, MAThe Senior Manager, Learning and Development position will be responsible for developing and implementing effective strategies and initiatives for learning and development that creates a model for all of BeiGene, encompassing leadership development for managers and professional development for non-managers. Human ResourcesDetail
Director and Senior Corporate Counsel, US ProductsEmeryville or, San Mateo CABeiGene is seeking an experienced healthcare law attorney to provide legal support, counseling and training related to the commercialization of BeiGene products in the United States. The attorney’s primary focus will be providing legal support, advice and training to the product/brand team, including Marketing, Sales and Medical Affairs. LegalDetail
Manager, Statistical ProgrammingSan Mateo, CA or Emeryville, 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
Global Head of Workplace ServicesSan Mateo, CA, Emeryville, CA, Cambridge, MA, Fort Lee, NJBeiGene is seeking a Global Head of Workplace Services to create and drive a BeiGene Workplace Strategy while at the same time overseeing all Real Estate, Facilities and Travel on a Global basis. Office of the CEODetail
Manager, IRT ValidationUS Remote, Cambridge, MA or Emeryville or Fort Lee, NJThe primary responsibility of the Manager, IRT Validation is to manage BeiGene’s companywide Interactive Response Technology (IRT) processes related to User Acceptance Testing. Responsible for identifying UAT requirements to ensure proper risk mitigation to ensure system is properly qualified for use. Leads UAT activities effectively and coordinates with team members across BeiGene sites and functions to support UAT. Global Clinical Development OperationsDetail
Manager, Drug Safety OperationsEmeryville, CA or San Mateo, CAAssist in the oversight of CRO responsible for global SAE case processing and submissionsDrug SafetyDetail
Senior Safety Specialist / Manager, PV Training & Quality ManagementEmeryville, CA or San Mateo, CAWorks with PV and Drug Safety team to ensure compliance of pharmacovigilance activities

Contributes to PV aspects of clinical trial activities
Pharmacovigilance & Drug SafetyDetail
Information Security AnalystEmeryville, CA; San Mateo, CA or Cambridge, MA. The Information Security Analyst (ISA) is an essential and instrumental part of the IT Security team providing hands-on day-to-day security administration along with conducting audits, assessments, investigations, training and operational duties.ITDetail
Associate Director Diagnostic Alliance ManagementSan Mateo, CA or Emeryville, CAThe Associate Director Diagnostic Alliance Management will support the review of potential Diagnostic partnership proposals, execution of such partnerships, and management of Joint Project Teams.Biomarker Development & Translational ResearchDetail
Medical Director/Senior Medical Director Safety ScienceSan Mateo, CA, Emeryville, CA, Cambridge, MA, Fort Lee, NJPerson in this position provides the medical input needed to interpret safety data derived from any source including clinical trials, literature, post marketing studies and post marketing spontaneous adverse event reports in order to identify and evaluate potential safety signals and develop appropriate risk mitigation strategies when a safety signal is confirmed.Drug SafetyDetail
Director, HRBPSan Mateo, CA or Emeryville, CAWe are looking for a dynamic, business-focused HR talent who brings to the role a love of life sciences, a curiosity which enables talent solutions and a strong consulting style in service of coaching and supporting leaders as they grow their organizations.Human ResourcesDetail
Director Licensing & Business DevelopmentCambridge, MA. Drive and coordinate the search, evaluation, and due diligence process to identify pre-clinical, clinical, and commercial stage opportunities in the field of Oncology and Immuno-OncologyLicensing & Business DevelopmentDetail
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
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
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
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
Senior Manager/Manager, GCP Quality AssuranceSan Mateo or Emeryville CAThe Manager of GCP 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
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/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
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
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
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