Jobs at BeiGene

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.

Responsible for global operational leadership of clinical studies, ensuring execution across regions and managing timelines, quality, and budget. Leads clinical operations team and collaborates with stakeholders for successful study execution and compliance. Oversees recruitment, data handling, and resource management; prepares for audits and drives improvements in efficiencies.

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 US brand strategy and annual planning, drive competitive readiness, manage brand budget and forecasts, partner with GIA on market research and insights, enable field and executive communications, and execute cross-functional strategic projects.

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 Senior Director of Program & Portfolio Governance drives program execution excellence and portfolio governance, aligning strategic objectives with operational execution across Global Technology Solutions.

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 Senior Manager, Data Steward (AI) will lead data stewardship initiatives in Pharma R&D, ensuring data quality and governance while mentoring a team and collaborating across departments to enhance data usability for insights and compliance.

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.

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.

Executive leader defining and executing enterprise AI and data strategy for a biotech company. Build data governance, LLM capabilities, and scalable AI frameworks; lead cross-disciplinary teams, enable organization-wide AI adoption through training and partnerships, and align AI initiatives with business objectives to drive innovation and patient-centric outcomes.