Effective March 17, 2025, The U.S. subsidiary of BeiGene, Ltd. has changed its name to BeOne Medicines USA, Inc. This change comes ahead of our anticipated global rebranding to BeOne Medicines Ltd. and redomiciliation to Switzerland, pending shareholder approval. The new name reflects our commitment to develop innovative medicines and partner with the global community to help as many patients with cancer as possible. To learn more about BeOne Medicines, please follow our new LinkedIn profile @BeOne Medicines.
Open Positions
Director, Global R&D Compliance
10+ years of experience in compliance, legal, or R&D, Bachelor's degree, strong understanding of global clinical development and research operations
Senior Director, GCO Franchise Head
Bachelor or higher degree in scientific or healthcare discipline, 12+ years' experience in clinical trial industry, leadership and people management experience, and global competencies
Regional Clinical Study Senior Manager
6+ years of experience in clinical research, proven experience as team lead in clinical functions, experience as CRA is preferred
Key Account Manager, UK
Life science degree, several years of commercial experience, and strong identification with BeOne's values
Senior Manager - Associate Director, Regulatory Affairs, Japan
10+ years of experience in the biotechnical or pharmaceutical industry, with a minimum of 5 years in a Regulatory capacity and 5 years working on development programs in Japan
Associate Director, Biostatistics (Central Statistical Monitoring)
6+ years of experience in biostatistics/statistics or related field, demonstrated experience in clinical trial statistics, and strong stakeholder management and communication skills
Regional Clinical Study Manager
4+ years of progressive experience in clinical research, Bachelor's Degree in a scientific or healthcare discipline, and excellent leadership and communication skills
Senior Analyst, QC Chemistry, US Site (Hopewell, NJ)
Bachelor’s degree in Chemistry, Biochemistry, or Biotechnology related scientific discipline and 4+ years of experience in FDA-regulated biotechnology, pharmaceutical company
Director, GCO Program Lead (GCPL)
10+ years of experience in clinical trial industry, Bachelor's degree in a scientific or healthcare discipline, Project management experience
Director, Oncology Program Manegement
10+ years of experience in drug development or commercial, 3+ years in leadership roles, PMP certification a plus
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