Jobs at BeiGene

Lead strategic planning, process improvement, and operations for the CMO Solid Tumors office. Manage cross-functional initiatives, resource and budget planning, vendor tracking, and dashboards; facilitate meetings and issue resolution; standardize processes and metrics to improve efficiency, quality, and performance across clinical development functions.

Manage clinical drug supply planning, label/pack and distribution for clinical studies. Develop and oversee supply and inventory plans, manage GMP inventory and vendor relationships, support IRT strategy and UAT, investigate exceptions and implement CAPAs, and lead cross-functional process improvements to ensure continuous patient supply and minimize waste.

Lead global distribution and trade operations for finished goods, APIs and drug products. Ensure cGMP/GSP/GDP compliance, manage carriers/3PLs, import/export/customs, temperature-controlled logistics, vendor performance, SOPs, ERP transactions (SOX-compliant), risk assessments, audits, and cross-functional coordination to support production schedules and continuous improvement.

The Associate Director, Regulatory Affairs will manage regulatory projects, provide strategic guidance, and ensure compliance with regulatory requirements while developing market access strategies for products.

The Senior Manager, Global Market Research will lead market research initiatives for BeOne's oncology products, support commercialization strategies, and deliver actionable insights to cross-functional teams.

The Senior Associate assists in the review and compliance of promotional materials for regulatory submissions, ensuring adherence to guidelines and collaboration with cross-functional teams.

Lead and develop clinical trial supply strategy within Global Supply Chain, ensuring timely drug supply and risk management while mentoring team members and collaborating cross-functionally.

The Director, GCO Clinical Program Lead (GCPL) is responsible for strategic leadership, program management, and oversight of early phase clinical trials, mentoring teams, and ensuring operational excellence.

The Regional Clinical Study Senior Manager is responsible for overseeing regional study delivery, managing clinical operations teams, ensuring compliance with quality standards, and collaborating with stakeholders on study progress and strategy.

The Associate Director, Compliance will manage compliance initiatives across North America, ensuring adherence to regulatory standards, providing guidance, training, and leading risk management efforts while promoting a culture of integrity.

Lead regional clinical operations for an assigned portfolio, ensuring timely, budgeted delivery and inspection readiness. Manage and mentor regional clinical study managers, align resources and vendors, drive feasibility, site selection, execution, data quality, SOP/work instruction development, and cross-functional collaboration. Oversee budgeting, forecasting, and stakeholder communications across region and support global study planning and clinical report activities.

Lead and manage regional clinical study management team, ensuring on-time, quality trial delivery. Oversee resourcing, capability development, SOP and risk adherence, stakeholder collaboration, budgeting, hiring, performance management, and continuous improvement across the region.

Lead the strategy and implementation of AI solutions in R&D, driving adoption and improving operational efficiency through advanced analytics. Collaborate with cross-functional teams to design AI/ML models and evaluate new technologies.

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 Executive Director is accountable for strategic operational planning and clinical performance in the Breast and Women's Cancers Franchise, leading a team while ensuring goal achievement and operational excellence.

The GCO Program Lead is responsible for strategic operational planning, program management, and leading clinical operations teams to ensure excellence in clinical trials. This role involves mentorship, resource management, and collaboration with cross-functional teams.

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 programming for multiple clinical development projects, ensuring quality and compliance while collaborating with cross-functional teams and overseeing data analysis.

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.

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.