Jobs at BeiGene

The Senior Manager, Treasury Solutions leads the Treasury and Cash Management capabilities at BeOne, overseeing the solution lifecycle, managing SAP systems, and collaborating on strategic initiatives to improve efficiency.

The role involves developing global pricing and market access strategies for Solid Tumor pipeline products and ensuring alignment with payer needs through cross-functional collaboration.

The Director will lead digital marketing strategies for Market Access, enhance digital platforms, collaborate across teams, and manage compliance and budgets.

Lead biostatistical support for hematology clinical trials: develop/implement SAPs, analyze and interpret trial data, collaborate with cross-functional teams, ensure regulatory-compliant programming and data quality, and contribute to manuscripts and submissions.

Lead the Central Statistical Monitoring team, ensuring subject safety and data integrity in clinical trials through statistical analysis and collaboration with various stakeholders.

The Manager R&D Data Steward oversees data governance, quality management, and stewardship of R&D data, ensuring compliance and integrity across data products and leading a team to support data management initiatives.

Lead statistical analyses for Real-World Data (RWD) and Evidence (RWE) studies, oversee programming deliverables, analyze large datasets, and provide statistical consultation for biostatistics projects.

The Director, Global Regulatory Project Management leads oncology regulatory strategies, ensuring successful global drug submissions, while driving operational excellence and collaboration across teams.

As a Senior Manager, R&D Data Steward, you will oversee stewardship of Pharma R&D data, ensuring data quality and compliance across the R&D value chain. You will lead a team, operationalize data governance, and drive improvements in data management processes, leveraging automation and cross-functional collaboration to enhance data-driven insights.

The Associate Director, Platform Engineering is responsible for building and maintaining a digital platform, overseeing engineering strategy, compliance, team mentorship, and cross-functional collaboration to ensure platform reliability and innovation.

Lead the Central Statistical Monitoring team to oversee statistical design and governance in clinical trials, ensuring data integrity and safety. Develop monitoring indicators, validate models, and communicate findings to cross-functional teams. Provide training and support for audits and inspections, promoting continuous improvement in statistical practices.

The Federal Account Director develops and implements strategic business plans for federal accounts, enhancing corporate relationships and market access in oncology.

The Federal Account Director will lead business planning and relationships with key oncology stakeholders, drive market access strategies, and coordinate with sales management to ensure effective contract implementation.

Lead and execute clinical study start-up activities (site selection to activation), manage ICF/submissions and central IRB filings, maintain CTMS and eTMF records, ensure regulatory and ICH/GCP compliance, streamline local workflows, and support continuous SSU process improvements to meet timelines and quality standards.

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.

Accountable for end-to-end global operational delivery of clinical studies. Serves as primary global operational owner, leads cross-functional and regional teams, manages timelines, enrollment, quality, budgets, risk mitigation, regulatory submissions, TMF oversight, vendor management, and ensures ICH/GCP compliance and inspection readiness.

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.

Lead and line-manage a team of Clinical Trial Management Associates, allocate resources to studies, drive process improvements, ensure operational excellence and compliance with ICH/GCP and SOPs, and support study teams with clinical operations tasks including eTMF, CTMS, EDC, and IRT activities.

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.

The Senior Director leads study start-up operations across North America, ensuring rapid site activation, managing budgets, and overseeing regulatory submissions while promoting continuous process improvements and team development.