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
Manager/Senior Manager, Safety ScienceSan Mateo, CA, Emeryville, CA, Ridgefield, NJ, Cambridge, MAThe 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 documents.Pharmacovigilance and Drug SafetyDetail
Equity & Payroll Administration ManagerCambridge, MA.The Equity Administrator is responsible for managing all aspects of the Company’s stock plan administration and stock-based compensation including stock options, restricted stock awards, restricted stock units, and ESPP. This is an excellent opportunity to build the function and continue to raise the bar, in terms of service delivery and customer satisfaction. This role reports to the U.S. Controller / Director of Accounting.Finance / AccountingDetail
Corporate Communications ManagerCambridge, MA.The Manager of Corporate Communications works to positively position the company with external and internal audiences outside China. The position is charged with implementing communications strategies and is responsible for supporting the positive reputation of the company through digital communications, public relations and other activities.The Manager of Corporate Communications will work to raise the organization’s visibility as a global oncology company. Reporting to the company's Director of Corporate Communications, the position is expected to have a full understanding of responsible communications practices to support of the company’s long-term goals.FinanceDetail
Assistant General Counsel, Business DevelopmentCambridge, MA; Emeryville, CA or, San Mateo, CAWe are seeking a highly accomplished transactional attorney with significant experience in structuring, drafting and negotiating complex licensing, collaboration and strategic transactions in the life sciences industry. This is a senior-level position. The most successful candidates will have experience at the partner or similar level at a top-tier law firm and/or as in-house counsel advising on, drafting and executing such transactions, with a high-volume and high-profile deal list.LegalDetail
Director / Senior Director, US Sales OperationsSan Mateo, CA, Emeryville, CA, remoteThe Director / Sr. Director, US Sales Operations will lead the design, development and implementation of BeiGene’s first sales operations function within the US. Reporting to the Vice President, US Commercial Operations and Business Analytics, this position will be a key driver in building and scaling the US Sales organization to support the commercialization of BeiGene’s oncology portfolio.

CommercialDetail
Director / Sr. Director, Patient Support ServicesSan Mateo, CA, Emeryville, CAThe Director / Sr. Director of Patient Support Services will lead the design, development and implementation of BeiGene’s inaugural patient support services offerings in the US. Reporting to the Vice President of US Market Access, the Director / Sr. Director of Patient Support Services will play a critical role in ensuring that patients have access to BeiGene products. This individual will be accountable for the overall US patient access services strategy and the performance of patient and provider support services for BeiGene. As BeiGene grows, the role may evolve to take on global (ex-China) activities as well.CommercialDetail
Senior Director, US Marketing, BGB-3111San Mateo, CA, Emeryville, CAThe Senior Director, BGB-3111 US Marketing is responsible for the development, implementation, management, and execution of a best-in-class promotional strategy to support the US launch of BGB-3111, BeiGene’s next generation BTK inhibitor. This position reports to the VP, US Marketing. As BeiGene grows, the role may evolve to take on global (ex-China) marketing activities as well.CommercialDetail
Vice President, US MarketingSan Mateo, CA or Emeryville, CAThe Vice President, US Marketing will build and lead the marketing function responsible for developing and executing commercialization strategies that support the launch of BeiGene’s oncology products within the US. The role will collaborate closely with cross-functional leaders, including Market Access, Sales, Commercial Operations, Business Analytics and Medical Affairs. As BeiGene grows, the role may evolve to take on global (ex-China) marketing activities as well.CommercialDetail
Vice President, US SalesRemoteThe Vice President, US Sales will build and lead a best-in-class sales organization responsible for achieving sales objectives for BeiGene’s oncology products within the US. The VP, Sales will collaborate with BeiGene leadership to develop commercialization strategies that enable the BeiGene oncology portfolio to meet its full revenue potential.CommercialDetail
Vice President, Commercial Operations & Business AnalyticsSan Mateo, CA or Emeryville, CAThe Vice President, Commercial Operations and Business Analytics will build and lead the commercial function responsible for establishing and maintaining the analytic and operational infrastructure for BeiGene’s US Oncology Commercial organization. This leader will play a key role in scaling the US commercial organization and will oversee individuals and teams responsible for forecasting, market research, competitive intelligence, commercial planning, data strategy, sale operations and meetings and events. As BeiGene grows, the role may evolve to take on global (ex-China) activities as well.CommercialDetail
Vice President, US Market AccessSan Mateo, CA, Emeryville, CA, Ridgefield, NJ, Cambridge, MA, RemoteThe Vice President, US Market Access will build and lead the commercial function responsible for delivering rapid and comprehensive access for new and existing products across BeiGene’s oncology portfolio. The VP, US Market Access will collaborate across the organization to develop and implement compelling payer value propositions and own the distribution, trade and channel strategy for BeiGene’s oncology products. As BeiGene grows, the role may evolve to take on global (ex-China) market access activities as well.CommercialDetail
Manager, Financial Planning & AnalysisCambridge, MAThe Manager, Financial Planning & Analysis (FP&A) will be primarily responsible for the corporate expense consolidation related to headcount, clinical trial and other external expenses. This role will be pivotal in the planning and budgeting processes such as the annual budget cycle, monthly reporting and quarterly reforecasts and our long range strategic planning efforts. The Manager of FP&A will be responsible for ongoing & new reporting initiatives, such as monthly actual results vs budget & forecasts, collaboration updates, KPI reporting package etc. This role will work closely with FP&A team across the globe to ensure key deliverables are achieved.FinanceDetail
AccountantCambridge, MAThis is a new position within the growing Accounting/Finance department of Beigene, located in Cambridge. The accountant will perform the accounting close and transaction activities including AP, payroll, fixed assets, account reconciliations, and other activities.Accounting/FinanceDetail
Director, Data Privacy and Security CounselCambridge, MA; Emeryville, CA; San Mateo, CA or, Ridgefield Park, NJWe are seeking a sophisticated data privacy and security specialist to complement BeiGene’s growing internal Legal & Compliance team as we further our vision to develop and commercialize molecularly targeted and immuno-oncology cancer therapeutics.Legal & ComplianceDetail
Director/Associate Director, Epidemiology/Health Economics and Outcomes Research (HEOR)Remote or San Mateo, CA or Emeryville, CAThis position will lead and manage epidemiology / health economics and outcomes research programs to ensure quality, time and budget deliverables to support Beigene’ products. Work closely with other functional groups by providing epidemiology and outcomes research leadership for observational research on the natural history of disease and comparative safety, effectiveness and cost of medical treatment.Medical AffairsDetail
Senior Manager/Associate Director, CMC Regulatory AffairsSan Mateo, CA or Emeryville, CAThe Associate Director, Regulatory Affairs CMC, is responsible for developing and implementing global regulatory CMC strategies to secure and maintain market access for assigned product(s) in line with business objectives, and in coordination with key internal stakeholders.Regulatory AffairsDetail
Director, IP CounselCambridge, MA; Emeryville, CA or San Mateo, CAWe are seeking an experienced IP counsel to support our R&D and commercialization efforts as we further our vision to develop and commercialize molecularly targeted and immuno-oncology cancer therapeutics. Legal & ComplianceDetail
AD/Director of Global ProcurementCambridge, MAThe AD/Director of Global Procurement is responsible for establishing, managing and improving all aspects of purchasing direct and indirect goods and services for BeiGene to gain the maximum value from our supplier relationships. The AD/Director of Global Procurement will lead the business by coordinating with various functions to ensure seamless purchasing and reporting in our new ERP environment (SAP S/4Hana).FinanceDetail
Senior Medical Writer/Medical WriterSan Mateo, CA or Emeryville, CA or RemoteThe 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. Clinical regulatory documents include, but are not limited to, study reports, clinical study protocols or amendments, investigator brochures, regulatory briefing documents, and clinical sections of INDs, NDAs, MAAs and other regulatory submission documents.Medical WritingDetail
Manager, Regulatory Technology - Reg OpsSan Mateo, CA or Emeryville, CAThe Manager, Regulatory Technology, Regulatory Affairs Operations is responsible for providing technical and system support to the growing Regulatory Operations team in BeiGene. This person will help to establish the Regulatory Technology Function.Regulatory AffairsDetail
Submissions Operations Management Sr. Manager, Reg OpsSan Mateo, CA or Emeryville, CAThe Submissions Operations Manager is responsible for providing publishing, technical editing and general submission support to the growing Regulatory Operations team. This person will help to establish the Submission Operation Management Function at BeiGene and help to establish an approach for regulatory submissions.Regulatory OperationsDetail
Sr. Manager Data Disclosure and TransparencySan Mateo, CA or Emeryville, CAWe have an exciting opportunity within our Regulatory Operations team for a Senior Manager who will be responsible for Clinical Trial Disclosure and Data Transparency Activities. These activities include coordinating disclosure, transparency and data sharing communication and outreach plans, monitoring the landscape to ensure that BeiGene’s data transparency policy is up to date, and creating key performance indication (KPI) reports that demonstrate adherence to regulations.Regulatory AffairsDetail
Associate, Regulatory Technology - Regulatory OperationsSan Mateo, CA or Emeryville, CAThe Associate, Regulatory Technology, Regulatory Affairs Operations is responsible for providing submission publishing and technical support of the Regulatory systems for BeiGene. This position provides global support to the Regulatory Affairs and Regulatory Operations organizations with an immediate focus of supporting technical projects and regional regulatory filings.Regulatory AffairsDetail
Senior Director, Clinical Data ManagementFull TimeSan Mateo, CA or Emeryville, CA or Ridgefield, NJ or Cambridge, MAIn this leadership position, the Senior Director, Clinical Data Management will manage operational aspects of data management supporting global drug development activities. This position will drive the strategy and lead clinical data management initiatives across multiple therapeutic portfolios, as well as manage the selection and oversight of data management vendor partners.BiometricsDetail
Head of Biostatistics: USAFull TimeSan Mateo, CA or Emeryville, CA or Ridgefield, NJ or Cambridge, MASupporting oncology clinical development, 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.BiometricsDetail
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 Ridgefield, 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 Ridgefield, 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
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, Ridgefield, 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 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
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, Ridgefield, 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 Ridgefield, 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, Ridgefield, 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
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 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