Jobs at BeiGene

Lead design and execution of primary market research for oncology pipeline; integrate primary and secondary data (market sizing, forecasting), deliver insights to cross-functional teams, manage vendors, and support commercialization strategy and business reviews to inform launch planning.

Lead global technology strategy for corporate enabling functions (HR, Legal, Communications, BD), drive AI and automation, ensure data governance and security, oversee enterprise platforms and vendor relationships, manage a global technology team, and partner with senior stakeholders to deliver scalable, compliant solutions.

The role involves leading a regional clinical study management team, ensuring trial delivery, maintaining quality standards, managing budgets, and mentoring staff in a biotech environment.

Design, develop, test, deploy, and maintain ETL data pipelines, validation checks, and data models for clinical trial data. Ensure data quality, governance, security, and performance; support analytics/BI consumers and collaborate with cross-functional clinical and IT stakeholders.

Lead and line-manage a CTMA team supporting clinical studies from start-up to close-out. Assign and onboard staff, ensure compliance with ICH/GCP and SOPs, maintain CTMS/EDC/IRT and eTMF, drive process improvements, and support clinical operations metrics and strategy.

Lead global tax strategy and cross-border planning for an IP-centric oncology company. Design tax-efficient structures for R&D, clinical trials, manufacturing, and commercialization; oversee transfer pricing, M&A tax structuring, tax forecasting, audits, and governance; manage external advisors and a global tax team while advising senior leadership and supporting compliance with OECD Pillar Two and other global tax rules.

Senior leader responsible for global tax reporting, ASC 740 accounting, compliance governance, and tax operating model transformation. Partners with Finance, Legal, Treasury and auditors to ensure accurate tax provision reporting, SOX controls, automation and AI adoption, and scalable processes across jurisdictions while leading a global tax team.

Lead global clinical operations for the Hematology franchise, managing GCPL/gCSM teams, strategic program planning, resource and budget forecasting, vendor governance, risk/issue escalation, and cross-functional collaboration to ensure clinical trial execution aligned with regulatory standards (ICH/GCP).

The Director of Business & Strategic Operations oversees internal operations, manages resources and budgets, drives operational excellence, and collaborates with clinical operations teams to optimize processes and ensure effective communication across departments.

Lead development and application of analytics, statistical models, and dashboards to support R&D Quality oversight. Integrate clinical, safety, lab, and operational data to identify risks, support audit/inspection readiness, enable RBQM, and provide actionable quality insights and recommendations to cross-functional partners.

Lead and manage Global Study Management Associates across regions, overseeing resourcing, training compliance, study delivery, quality and inspection readiness, process improvement, stakeholder collaboration, and team development. Drive operational excellence, mentor staff, support hiring, and ensure alignment with regulatory standards and organizational strategy.

Lead global strategic feasibility for clinical studies by integrating regional data, tools, and stakeholder input to inform country/site selection, recruitment and retention strategies, predictive modelling, risk/mitigation plans, and operational recommendations supporting study design and execution across development stages.

Lead execution and scaling of North America compliance program through operations, governance, analytics, and cross-functional projects. Build dashboards and monitoring to identify risks, support audits/investigations, improve controls and documentation, and embed compliance into business initiatives while partnering with Legal, Commercial, Medical Affairs, Finance, HR and other stakeholders.

The role leads cost optimization and innovation initiatives in R&D, ensuring effective budget management and collaboration across teams. It emphasizes data-driven insights and strong analytical capabilities.

Lead regional site feasibility and enablement for the Americas, defining strategy, driving site selection and enrollment forecasting, building site partnerships, expanding trial access, implementing feasibility tools and recruitment programs, managing cross-functional teams, and improving processes to accelerate study startup and enrollment across the clinical portfolio.

The Senior Clinical Research Associate manages clinical study sites, ensuring compliance with protocols, mentoring CRAs, and optimizing study performance while adhering to regulatory standards.

Lead category management for CRO and FSP outsourcing, partner with R&D to define sourcing strategies, identify cost optimization opportunities, manage vendor selection and contracting (MSA/rate cards), oversee supplier relationships, performance, risk, and governance, and support implementation of sourcing initiatives and digital/AI-enabled solutions.

Lead global commercial strategy and launch readiness for two late-stage lung cancer assets. Mobilize and direct Global Brand Teams, align cross-functional stakeholders (R&D, Medical, Tech Ops, Regions), drive annual and long-range planning, translate clinical evidence into a global narrative, manage competitive strategy, and develop talent to achieve commercial launch and lifecycle growth objectives.

Lead end-to-end lifecycle management of Global Clinical Operations external systems (CTMS, eTMF, IRT, EDC, SSU). Oversee implementations, maintenance, security, vendor/SLA management, budgets, compliance (21 CFR Part 11, GAMP), data integrity, incident response, documentation, training, and cross-functional integration. Develop roadmaps, business cases, and governance while managing and developing a global systems team.

Lead Global Clinical Operations quality, compliance, and process excellence. Build and manage a team to implement GCP-compliant systems (including eTMF), SOPs, KPIs/KQIs, training, CAPA, and inspection preparedness. Partner with QA, Compliance, and cross-functional stakeholders to drive continuous improvement, vendor due diligence, and clinical trial oversight worldwide.