Jobs at BeiGene

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.

Manages clinical trial drug supply activities, including demand planning, supply and inventory plans, production schedules, labeling, packaging, comparator sourcing, IRT strategy and testing, shipment coordination, and import licenses. Collaborates with clinical operations, regulatory, quality, CMC teams, CMOs, depots, vendors, and study stakeholders to ensure continuous patient supply, minimize waste, monitor schedules, and mitigate risks.

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.

Supports country and site feasibility for clinical trials by analyzing internal data, evaluating investigators and sites, coordinating feasibility outreach, resolving site-selection issues, and preparing assessments and meeting materials. Maintains site databases and feasibility resources, collaborates with Clinical Operations, Data Sciences, Medical Affairs, and external partners, supports investigator engagement and enrollment planning, and contributes to process improvements, training, and standardized feasibility methodologies.

Accounting Manager responsible for daily accounting operations, general ledger governance, fixed asset accounting, and monthly and quarterly close processes. Leads financial reporting, reconciliations, journal review, audits, SOX 404 controls, and US GAAP compliance. Partners with finance, tax, purchasing, shared services, and external auditors while driving process automation and continuous improvement. Provides functional oversight to shared-service accounting resources and supports cross-functional finance initiatives.

Leads clinical monitoring operations and CRA team performance across clinical trials, ensuring ICH-GCP, regulatory, and SOP compliance. Responsibilities include resource allocation, quality oversight, audits, inspections, expense management, site relationships, risk resolution, mentoring, recruitment, performance management, and cross-functional clinical operations initiatives. The role requires strong knowledge of drug development, monitoring, trial execution, and oncology, along with significant pharmaceutical, CRO, or biotech experience.

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 digital clinical operations capabilities across the clinical trial lifecycle, focusing on CTMS enhancements, process optimization, requirements gathering, prioritization, roadmaps, user acceptance testing, and technology value realization. Partners with Clinical Operations, IT, Development, QA, and vendors to deliver compliant, efficient, and innovative solutions. Manages stakeholder communications, champions, backlogs, business outcomes, change adoption, and project progress while supporting validated systems and clinical operations technology.

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.