Jobs at BeiGene

Provides strategic intellectual property counsel for biologic products, supporting R&D, manufacturing, business development, and commercialization. Responsibilities include building patent portfolios, conducting patentability and freedom-to-operate analyses, monitoring global patent law, supporting collaborations and transactions, reviewing publications, advising on regulatory exclusivity and trademarks, and assisting with litigation. The role requires extensive biopharmaceutical patent experience and collaboration with scientific and business leaders.

Own the quantitative and analytical foundation for R&D portfolio prioritization, valuation, resource optimization, and governance. Develop eNPV and probability-of-success models, integrate scenarios and competitive intelligence, and translate complex analyses into executive-ready recommendations. Partner with finance, commercial, program management, data science, and governance teams to build reusable dashboards, predictive tools, AI-enabled workflows, and consistent portfolio decision processes.

Lead Program & Study Management (P&SM) operations to drive process optimization, operational excellence, and strategic initiatives for global clinical study execution. Identify improvement opportunities, implement change, align cross-functional teams, ensure ICH/GCP and regulatory compliance, and develop training to enhance clinical project management capabilities. Influence long-term strategy and support global study teams while managing resources, budgets, and performance tracking.

Leads global portfolio and project management for external drug development partnerships, overseeing clinical development and commercialization lifecycles, project plans, milestones, budgets, KPIs, risks, governance, alliance management, and cross-functional collaboration. Drives process improvement, operational efficiency, strategic decision-making, partner onboarding, and high-quality execution across international teams. Supports oncology and hematology development initiatives while coordinating advisory committees and global R&D stakeholders.

Leads enterprise legal entity planning, forecasting, reporting, governance, and reconciliation with consolidated FP&A forecasts. Partners with Tax, Treasury, Accounting, Finance Systems, and business teams to support tax planning, transfer pricing, liquidity forecasting, cash allocation, variance analysis, and executive decision-making. Builds scalable TM1 forecasting capabilities, establishes controls and accountability, and translates entity-level financial data into actionable insights.

Leads global Microsoft 365 strategy, platform engineering, architecture, governance, reliability, security, lifecycle management, migrations, Copilot enablement, integrations, and commercial oversight. Manages distributed teams and partners while establishing product ownership, support models, enterprise controls, service performance standards, and modernization plans. Requires executive judgment, Microsoft 365 technical depth, global transformation experience, licensing expertise, and leadership in complex regulated environments.

Oversees clinical monitoring activities and CRA performance to ensure compliance with ICH-GCP, regulations, and company SOPs. Manages CRA resource allocation, quality indicators, site relationships, audits, inspections, risk resolution, and milestone delivery. Leads recruitment, onboarding, task assignment, performance evaluations, mentoring, and professional development for the CRA team. Supports monitoring competency assessments and cross-functional collaboration across clinical trials.

Leads global strategic feasibility and study start-up activities for clinical studies. Oversees feasibility planning, enrollment forecasting, study documentation, process optimization, risk management, vendor and site partnerships, and cross-functional collaboration. Builds and manages a global team, standardizes tools and processes, analyzes data for study decisions, and presents recommendations to senior leadership. Requires substantial clinical development, study operations, process improvement, and people leadership experience.

Leads global clinical process management within Global Clinical Operations, ensuring efficient, consistent, sustainable, and compliant processes aligned with ICH-GCP and regulatory requirements. Responsibilities include owning and developing SOPs and work instructions, leading process improvement and change initiatives, managing document approvals, supporting implementation and training, and collaborating with global and cross-functional stakeholders in a matrix environment.

Manages clinical trial data from study startup through database lock and clinical study report support. Leads studies, oversees internal and CRO/FSP data management resources, develops eCRFs and edit checks, manages EDC database testing, coordinates data cleaning and reconciliation, supports coding and medical review, ensures regulatory and quality compliance, and contributes to process improvement and team mentoring.

Manages clinical trial data activities from study startup through database lock, including data cleaning, query management, reconciliation, reporting, documentation, database build support, UAT, and data review. Coordinates with study teams, vendors, laboratories, and database builders; identifies and escalates data issues; supports regulatory and SOP compliance; and may lead studies, mentor team members, and train personnel on EDC and eCRF processes.

Leads hematology portfolio strategy and governance across R&D, Commercial, Finance, and executive leadership. Manages development review committee processes, portfolio prioritization, strategic decision-making, executive materials, risk escalation, and action tracking. Translates scientific, clinical, competitive, operational, and financial information into recommendations for investment, development pathways, lifecycle planning, and portfolio differentiation. Builds alignment among senior stakeholders and improves governance processes in a global, matrixed pharmaceutical environment.

Leads BeOne’s global organizational change management strategy across technology, enterprise platforms, AI adoption, ERP, GBS, and operating model transformations. Advises executives, oversees portfolio change governance, builds an OCM center of excellence, drives readiness, adoption, communications, and value realization, and leads a globally distributed team. The role requires extensive enterprise transformation experience, executive influence, global leadership, life sciences experience, and fluency in change methodologies and enterprise technologies.

Owns and leads commercial master data management across HCP, HCO, payer, patient, product, and organizational domains. Establishes governance frameworks, stewardship programs, data quality standards, matching and survivorship rules, and trusted golden records. Manages commercial data platforms, integrations, analytics datasets, releases, vendors, and offshore teams. Writes SQL, builds validations and data pipelines, troubleshoots integrations, supports commercial launches, and drives operational improvements across pharmaceutical commercial systems.

Owns the development, governance, integration, and enhancement of clinical trial resource and costing systems for Phase I–III studies. Develops costing algorithms, maintains assumptions and benchmarks, coordinates integrations with CTMS, EDC, SAP, Workday, and other enterprise systems, and supports testing, reporting, dashboards, training, and compliance. Partners with Clinical Operations, Resource Management, Finance, HR, IT, and strategic sourcing to improve cost estimation, resource forecasting, pricing insights, and operational efficiency.

Manages companion diagnostic (CDx) portfolio and project activities within the Precision Medicine Team. Responsibilities include coordinating diagnostic partner engagement, project scoping, contracts, budgets, forecasts, timelines, risks, documentation, governance, and cross-functional communications. The role maintains portfolio tracking tools and supports CDx collaboration execution across internal stakeholders and external partners.

Leads global clinical biomarker and translational medicine strategies for solid tumor oncology programs. Oversees biomarker assay development, validation, data analysis, companion diagnostic initiatives, regulatory contributions, and clinical trial advancement. Partners with cross-functional teams, CROs, academic institutions, and industry collaborators while translating biomarker findings into development recommendations. Requires scientific leadership, oncology biomarker expertise, publication or regulatory experience, mentoring capability, and Mandarin proficiency.

Supports hematology clinical studies through protocol and statistical analysis plan development, database review, clinical trial data analysis, regulatory submissions, and clinical study reports. Collaborates with clinical, regulatory, programming, and data management teams; interprets results; responds to study-related queries; contributes to manuscripts and presentations; and supports innovative statistical methods in clinical development.

Leads R&D data stewardship across metadata, cataloging, data products, profiling, quality, governance, and compliance. Uses Informatica, SQL, Databricks, Python, and PySpark to curate data, automate workflows, define quality controls, and resolve complex issues. Applies AI-assisted stewardship and semantic data concepts while collaborating with technical and business stakeholders. Coaches other stewards, supports audit readiness, and improves stewardship standards and operating practices.

Leads global commercial strategy, launch readiness, brand planning, and lifecycle management for an oncology asset. Builds and directs a cross-functional Global Brand Team, aligns R&D, commercial, regional, and affiliate stakeholders, develops competitive and growth strategies, translates clinical evidence into market narratives, and supports global commercialization, supply planning, and stakeholder communications.