
Job Overview
Location
Remote (US)
Job Type
Full-time
Category
Human Resources
Date Posted
March 19, 2026
Full Job Description
š Description
- ⢠As Senior Director, Head of Global Clinical Process Management at BeiGene, Ltd., you will lead the design, implementation, and optimization of end-to-end clinical trial processes across global regions, ensuring operational excellence, regulatory compliance, and seamless execution of oncology trials. Your leadership will directly impact the speed, quality, and efficiency of bringing life-saving cancer therapies to patients worldwide by aligning people, process, and technology across Clinical Development, Global Process Owners, and cross-functional partners.
- ⢠You will strategically assess current clinical operations processes, systems, and infrastructure; conduct gap analyses; identify risks to inspection readiness; and operationalize mitigation strategies in collaboration with stakeholders. You will lead process improvement teams, develop future-state strategies, chair the SOP Governance Board, monitor key metrics, and drive organizational change management to ensure continuous improvement and alignment with global clinical trial standards.
- ⢠You will partner with Clinical Development, Data Management, Quality, Regulatory, and CROs to design integrated processes with clear inputs, outputs, and roles & responsibilities; facilitate leadership alignment on cross-functional SOPs; capture and communicate lessons learned; and optimize key process interfaces between internal and external teams to ensure seamless trial execution across geographies.
- ⢠BeiGene is a rapidly growing global biotechnology company dedicated to developing affordable, innovative cancer medicines. You will join a mission-driven organization where scientific rigor, collaborative spirit, and bold ingenuity are core values, and where your expertise will directly contribute to expanding access to oncology treatments for patients worldwide.
- ⢠In this role, you will develop deep expertise in global clinical operations excellence, influence enterprise-wide process strategy, mentor and develop high-performing teams, and gain visibility as a key leader on the Clinical Operations Excellence (COE) Leadership Teamāshaping the future of clinical trial execution at a pivotal stage in BeiGeneās growth.
šÆ Requirements
- ⢠Bachelorās degree with minimum 12+ years of experience in pharmaceutical or biotechnology drug development; Masterās degree preferred.
- ⢠Deep experience and expertise in end-to-end clinical trial processes, including hands-on experience in one or more key functions such as clinical research, clinical operations, data management, biostatistics, or project management.
- ⢠Proven experience in clinical trial process design, harmonization, optimization, and implementation, preferably in mid/large pharma or biotech settings with exposure to ICH GCP and regulatory requirements (FDA, MHRA/EMA).
- ⢠Strong leadership, collaboration, and influencing skills in complex, matrix environments, including direct experience mentoring, coaching, and managing performance of direct and indirect reports.
- ⢠Proficiency in Microsoft Suite (Excel, Outlook, Word, PowerPoint, Project); Six Sigma certification and/or experience with process mapping tools (e.g., Visio) desirable.
- ⢠Demonstrated ability to work effectively in cross-functional, global environments with 10-20% travel expected.
šļø Benefits
- ⢠Competitive base salary range of $206,200.00 - $276,200.00 annually, with eligibility for annual bonus and discretionary equity awards.
- ⢠Comprehensive benefits package including Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness programs.
- ⢠Opportunity to participate in the Employee Stock Purchase Plan and receive discretionary equity awards in BeGene, Ltd.
- ⢠Commitment to fair and equitable compensation practices, with packages tailored to individual skills, experience, and location.
- ⢠Equal opportunity employer with robust accommodations support for applicants requiring reasonable adjustments under Section 503, VEVRAA, ADA, and other applicable laws.
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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