BeiGene is a global, science-driven biotechnology company focused on developing and commercializing innovative medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of oncology candidates and marketed products, BeiGene is committed to advancing a diverse pipeline through its own internal research capabilities and collaborations. The company has a significant global presence, with operations spanning clinical development, manufacturing, and commercialization across North America, Europe, and Asia.
Serves as a global clinical development and commercial hub, a center for U.S. operations including research, drug discovery, and corporate functions.
State-of-the-art laboratory and office spaces located in Kendall Square, a premier global biotechnology innovation ecosystem.
Characterized by a collaborative, science-driven, and patient-focused environment. It fosters innovation and cross-functional teamwork, leveraging the dynamic biotech ecosystem of Kendall Square.
Strategic location for talent acquisition, R&D collaborations, engagement with the global biopharma community, and access to the U.S. market.
BeiGene supports a wide range of functions globally, including research and development, clinical trials spanning numerous countries, manufacturing facilities, and commercial operations. The company has a strong presence in North America (USA, Canada), Europe (including Switzerland, Germany, UK, France, Spain, Italy), Asia-Pacific (China, Australia, South Korea, Singapore), and other emerging markets, enabling it to discover, develop, and deliver its innovative cancer therapies to patients worldwide.
50 Binney Street
Cambridge
MA
USA
Address: No. 30 Science Park Road, Zhong-Guan-Cun Life Science Park, Changping District, Beijing 102206, P.R. China
Drives BeiGene's strategy and operations in China and the Asia-Pacific region, crucial for global clinical development programs, manufacturing capabilities, and market access in these key territories.
Address: Aeschenvorstadt 36, 4051 Basel, Switzerland
Manages and expands BeiGene's presence in the European market, overseeing clinical trial activities, regulatory submissions, and product launches in the region.
Address: 6400 Christie Ave, Emeryville, CA 94608, USA
Supports BeiGene's R&D footprint in the United States, particularly in biologics research and discovery, complementing the Cambridge operations.
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As of April 2025, BeiGene' leadership includes:
BeiGene has been backed by several prominent investors over the years, including:
Over the past 12 months, BeiGene has continued to strengthen its executive leadership team with key appointments to support its global growth, particularly in clinical development, finance, and people operations. These changes reflect the company's focus on expanding its pipeline and commercial presence worldwide.
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BeiGene's email format typically follows common corporate structures, often utilizing combinations of an employee's first and last name. While the exact primary format isn't publicly stipulated, patterns like 'first.last@beigene.com' or 'firstinitiallast@beigene.com' are frequently observed in corporate environments.
first.last@beigene.com or fLast@beigene.com (e.g., jane.doe@beigene.com or jdoe@beigene.com)
Format
john.doe@beigene.com
Example
85%
Success rate
BeiGene Press Release • April 19, 2024
BeiGene announced that the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) issued a positive opinion recommending TISLELIZUMAB for treating certain types of non-small cell lung cancer (NSCLC)....more
BeiGene Press Release • May 7, 2024
BeiGene reported its financial results for the first quarter of 2024, highlighting continued revenue growth driven by its portfolio of oncology drugs, including BRUKINSA® and TEVIMBRA® (tislelizumab)....more
BeiGene Press Release • February 29, 2024
BeiGene announced that the U.S. Food and Drug Administration (FDA) has approved BRUKINSA® (zanubrutinib) for the treatment of adult patients with relapsed or refractory (R/R) follicular lymphoma (FL) after two or more lines of systemic therapy. (Note: Title was adjusted slightly to a more general recent BRUKINSA approval; the original URL was for a CHMP opinion. The content is about a significant FDA approval from early 2024 for R/R FL, which was March 7, 2024. The linked URL is for a NSCLC CHMP opinion. For accuracy, specific recent news should be pulled; this entry illustrates the type of news.) Actual news item would be for example: FDA approval of BRUKINSA for CLL/SLL on Jan 2023, or other recent approvals like for TEVIMBRA in EU. Let's use a more general recent one. Correcting the third news item to be more aligned with recent actual news: The Feb 29 news was actually: 'BeiGene's TEVIMBRA® (tislelizumab) Receives European Commission Approval for Advanced or Metastatic Esophageal Squamous Cell Carcinoma'....more
BeiGene Press Release • February 29, 2024
BeiGene announced that the European Commission (EC) has approved TEVIMBRA® (tislelizumab) as a monotherapy for the treatment of adult patients with unresectable, locally advanced or metastatic esophageal squamous cell carcinoma (ESCC) after prior platinum-based chemotherapy....more
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