Jobs at BeiGene

Responsible for designing and implementing data governance capabilities in R&D, collaborating with stakeholders to ensure compliance and optimize data management across clinical domains.

Support implementation of the Culture of Quality program, enhance Quality communications (webpage, newsletters, sessions), create a Quality department storyboard, produce graphic and digital content, collect and analyze data, and collaborate cross-functionally to advance quality initiatives.

Lead global strategic feasibility for clinical studies by integrating internal and external data, advising country/site selection, recruitment and operational strategies, improving feasibility processes and tools, and partnering with program and study teams to optimize study design and execution across early to late-stage programs.

The Associate Director will drive digital tool adoption, develop communication strategies, train users, monitor progress, and oversee AI capabilities in Quality processes.

Lead the U.S. Biologics Regulatory CMC organization, develop global CMC regulatory strategies, oversee CMC submissions and health authority interactions, manage a ~15-person team, ensure compliance and inspection readiness, and support lifecycle management for biologics including mAbs, ADCs, cell therapies, and combination products.

The Executive Director leads Global Clinical Pharmacology & Development Technology Solutions, overseeing technology strategy, solution delivery, and team leadership to support R&D initiatives in cancer treatment.

The Associate Director drives analytics solutions for Clinical Operations, enhancing productivity, reducing inefficiencies, and aligning business needs with advanced analytics capabilities. They lead the enhancement of the analytics platform, manage stakeholder communication, and contribute to system testing and project leadership.

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 Senior Manager, Digital Quality Management Systems Business Analyst leads system implementations, manages quality digital tools, and coordinates cross-functional initiatives to ensure compliance and optimize processes.

The Sr Manager of Clinical Supply Chain oversees drug supply activities, manages relationships with stakeholders, ensures supply continuity, and leads process improvements.

The Director, Clinical Development oversees clinical programs in oncology, ensuring successful strategy execution, managing studies, and collaborating across functions and organizations to improve cancer treatment.

The role involves leading global forecasting and performance management, setting standards, overseeing processes, collaborating with cross-functional teams, and developing a high-performing team in the oncology biotech sector.

The Manager of Clinical Supply Chain oversees drug supply activities, developing supply plans, managing inventory, and ensuring compliance with regulations while collaborating with internal and external stakeholders.

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 Executive Director will lead global commercial strategies for TEVIMBRA, oversee cross-functional teams, and ensure alignment with business objectives to drive brand growth in oncology/hematology.

Lead and mentor oncology program management teams, develop global product strategies, manage projects, and drive process improvements in drug development.

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 Associate Director leads regional strategic feasibility in clinical operations, ensuring data-driven assessments, site recruitment, and stakeholder collaboration for successful trial execution.

The intern will assist in regulatory projects related to CMC, support document preparation, maintain regulatory information, and contribute to process improvements while gaining hands-on biotech experience.

The Sr. Director, Market Access Strategic Marketing develops and executes strategic marketing plans for products, aligns field teams, and collaborates across departments to optimize market access support and competitive positioning.