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, GCO Program Lead (GCPL)
10+ years of experience in clinical trial industry, Bachelor's degree in a scientific or healthcare discipline, Project management experience
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
Director, Global Regulatory Lead
BS degree or higher, 10+ years of experience in biotech/pharmaceutical industry, and 5+ years of experience in regulatory capacity
Associate Director, Regional Clinical Study Management
8+ years of experience in clinical operations, leadership and management experience, strong communication skills
Medical Science Liaison/Sr. Medical Science Liaison, Haematology
PhD, M.D. physician, DPharm, prior MSL experience, relevant industry experience in medical affairs, and ability to travel
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
Global Clinical Study Manager
5+ years of clinical research experience, project management experience in global pediatric studies, and advanced knowledge of clinical operations methodologies
Executive Medical Director, Safety Franchise Area Lead
10+ years pharmaceutical/biotechnology industry experience in Clinical Research, Clinical Development with at least 6 years in pharmacovigilance
Associate Director, Regulatory CMC (Small Molecule)
8+ years of related pharmaceutical or biopharmaceutical industry regulatory CMC experience. BA/BS Degree in scientific disciplines, MS/PhD preferred
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