Job Overview
Location
Remote (US)
Job Type
Full-time
Category
HR & Recruiting
Date Posted
May 10, 2026
Full Job Description
đź“‹ Description
- • The Director, Global Regulatory Lead at BeiGene, Ltd. is responsible for developing and implementing global regulatory strategies to secure and maintain market access for oncology products, ensuring alignment with business objectives and coordination with internal stakeholders.
- • Day-to-day responsibilities include providing strategic regulatory leadership for development programs, managing regulatory aspects of compounds through all phases of development and post-approval, preparing and submitting global regulatory documentation, interfacing with health authorities, leading cross-functional teams, and mentoring regulatory professionals.
- • BeiGene is a rapidly growing global biotechnology company focused on developing innovative medicines to fight cancer, with a commitment to scientific excellence, collaboration, and patient-centric values.
- • In this role, the individual will deepen expertise in global regulatory affairs, lead high-impact oncology development programs, influence corporate strategy through regulatory insight, and build leadership capabilities in a dynamic, mission-driven environment.
🎯 Requirements
- • BS with 10+ years, MS with 7+ years, or PhD/MD/PharmD with 5+ years of experience in biotechnology or pharmaceutical industry, including 5+ years in a regulatory capacity
- • Experience working as a regulatory lead across two or more major geographic areas, with prior experience in both small molecules and biologics
- • Thorough understanding of drug development process, regulatory requirements (INDs/CTAs, NDAs/BLAs/MAAs), lifecycle management, and health authority interactions
- • Strong business acumen, strategic thinking, and ability to balance short-term needs with long-term vision in a cross-functional environment
- • Excellent interpersonal, oral, and written communication skills, with proven ability to negotiate, build trust, and manage multiple projects simultaneously
- • Strong PC literacy with proficiency in MS Office (Outlook, Word, Excel, PowerPoint) and willingness to travel 10-20%
🏖️ Benefits
- • Comprehensive benefits package including Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness programs
- • Opportunity to own shares of BeiGene Ltd. stock through discretionary equity awards and Employee Stock Purchase Plan
- • Eligibility to participate in annual bonus or incentive compensation plans based on role classification
- • Commitment to fair and equitable compensation with salary range of $176,000 - $236,000 annually
- • Equal opportunity employer with support for reasonable accommodations under federal accessibility laws
- • Culture emphasizing Patients First, Driving Excellence, Bold Ingenuity, and Collaborative Spirit through twelve global competencies
Skills & Technologies
About BeiGene, Ltd.
BeiGene is a global biotechnology company discovering, developing, manufacturing and commercializing innovative oncology medicines. Its broad pipeline includes more than 50 clinical-stage molecules, spanning targeted therapy, immuno-oncology and combination regimens. Core products are BTK inhibitor BRUKINSA, PD-1 antibody tislelizumab and PARP inhibitor pamiparib, marketed worldwide through internal teams and strategic alliances. BeiGene operates integrated research campuses in Beijing and Cambridge, MA, a manufacturing facility in Suzhou and offices across North America, Europe and Asia-Pacific, serving patients in more than 45 countries.
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