BeOne Medicines

Artificial Intelligence

• Lead stewardship of critical Pharma R&D data domains, ensuring data quality, compliance, and usability across the research and development value chain.
• Lead / mentor a team of data stewards and partner closely with governance, data product, and business domain leaders.
• Operationalize data standards, resolve data issues, and deliver trusted, governed data products.
• Oversee the implementation and management of MDM initiatives while ensuring accurate, consistent, and complete data across the organization.

Senior Manager, Data Steward – AI

Clinical Operations

• Serve as a strategic liaison between Global Clinical Operations (GCO) and analytics delivery teams
• Lead the ongoing maintenance and enhancement of the Clinical Operations Analytics platform
• Translate business needs into actionable analytics solutions
• Oversee demand intake and prioritization
• Define and communicate the value proposition for analytics initiatives
• Establish and maintain communication channels to support knowledge sharing
• Contribute to the strategic roadmap for Clinical Operations Analytics

Associate Director, Business Analyst – Clinical Operations, Analytics

Business Analyst

• Serve as the business System Owner for assigned Quality GxP digital systems (e.g., eQMS, QualityDocs, etc)
• Lead and manage full lifecycle of system implementations and enhancements
• Gather and translate complex business needs into functional and technical requirements
• Drive process mapping, continuous improvement, and digital transformation initiatives across Quality
• Collaborate with cross-functional teams including QA, IT, Regulatory, Clinical, and external vendors to align systems with business strategy
• Develop and maintain strong relationships with business process owners
• Plan and lead UAT, training, and change management activities for new system features or implementations
• Manage project scope, timeline, resources, budgets, and risks
• Ensure ongoing system compliance with applicable GxP, FDA, EMA, and ISO standards
• Prepare and deliver high-quality project updates, stakeholder communications, and system documentation
• Oversee the governance, configuration, and administration of digital quality tools such as Veeva QMS

Senior Manager, Digital Quality Management Systems, Business Analyst

Compliance

• Support the development and implementation of the Company’s Healthcare Compliance Program in France
• Collaborate with internal teams to identify required regulatory submissions
• Deliver training to teams on regulatory submission processes
• Provide advice and guidance on healthcare compliance matters

Senior Manager, Healthcare Compliance

• Act as the local compliance officer for Germany
• Support development of Healthcare Compliance Program
• Collaborate with internal teams to ensure compliance with regulations
• Conduct monitoring and auditing of compliance policies
• Provide training on compliance matters

Associate Director, Healthcare Compliance

Manager

• Develop and execute strong regional plans with cross-functional support
• Support and develop trusted partnerships internally and externally
• Collaborate with health system partners and healthcare practitioners
• Establish superior working relationships with key opinion leaders
• Train and educate HCP’s on the proper use and handling of products
• Responsible for achieving related regional business and sales goals

Regional Manager, Hematology

Human Resources

• Adapt and implement global talent programs for Europe
• Drive regional talent strategy to support growth
• Support HRBPs in all talent processes
• Enable a culture of continuous feedback and development
• Use people analytics to identify trends and opportunities
• Drive regional adaptation of global engagement strategies
• Define success metrics and track program impact
• Advise HRBPs and business leaders using data-driven insights

Associate Director, Global Talent Management

Director

• Provide strategic leadership for TEVIMBRA, overseeing global commercial strategies, serving as the commercial voice at the Global Product Team (GPT), and representing the Brand across BeOne territories, with senior leadership, and with external stakeholders.
• Lead the Global Brand Team (GBT) ensuring productive information exchange and best practice sharing between GPT, GBT, and regional / affiliate team members.
• Develop an aligned view of brand growth drivers and ensure progress to plan consistent with agreed business objectives.
• Represent ONE commercial voice to Global Product Team (GPT), R&D, Tech Ops, Executive Leadership, and Solid Tumor Franchise Teams to drive organizational alignment and progress.
• Lead key cross-functional processes including the Annual Brand Plan, the Annual Operating Plan (AOP), and the Long-Range Plan (LRP) processes.
• Collaborate with cross-regional and cross-functional team members to shape brand strategies for multiple indications.
• Integrate major market input into global launch readiness plans and support the implementation / execution of global commercial strategies in local markets.
• Ensure long-term growth by translating complex clinical evidence into a unified global narrative that drives market leadership.
• Consolidate competitor understanding that spans multiple disease areas/indications into a cohesive product view.
• Develop succinct competitive response plans that are grounded in a deep understanding of marketplace performance and competitor strategies.
• Collaborate with functional leads to ensure insight generation that helps drive business performance and develop and maintain a Global Brand Dashboard.
• Identify barriers to brand adoption and develop plans to deliver continued brand growth.
• Drive value maximization and recommend growth strategies to meet long-term Solid Tumor portfolio ambitions.
• Collaborate with Regions and Corporate Communications to craft and refine stakeholder communications.
• Partner with Tech Ops to ensure optimized supply and demand management.
• Maintain strong relationships with both internal colleagues and external customers to address market opportunities.

Executive Director, Global Commercial Lead

Medical Director

• Work with Cross-functional teams to develop robust territory plans that impact and inform HCPs leading to improved patient outcomes
• Establish and maintain scientifically credible peer-to-peer scientific relationships with national & regional opinion leaders in addition to other healthcare providers
• Facilitate & monitor strategic partnerships with scientific/clinical experts and serve as an enterprise-level point of contact with organizations
• Support major and regional congresses by engaging thought leaders
• Provide balanced, accurate information to regional formulary decision makers and/or P&T committee members
• Identify and vet investigators, nominate sites to Clinical Operations for company-sponsored clinical trials as requested
• Assist in the development and execution of clinically relevant regional medical meetings

Field Medical Director – Solid Tumor, Breast and Lung

• Support BeOne Medicines pre-clinical and clinical pipeline development by coordinating external collaborations
• Establish and maintain scientifically credible peer-to-peer scientific relationships with national & regional opinion leaders
• Facilitate & monitor strategic partnerships with scientific/clinical experts
• Provide balanced, accurate information to regional formulary decision makers
• Identify and vet investigators, nominate sites to Clinical Operations for company-sponsored clinical trials
• Assist in the development and execution of clinically relevant regional medical meetings
• Serve as an internal resource of clinical and scientific information from medical interactions
• Build strong relationships with internal experts

• Serve as the lead bioinformatics scientist for internal drug discovery and development programs
• Provide comprehensive hands-on support for new target exploration and validation
• Design, develop, and deploy effective bioinformatics workflows and interactive tools to analyze high-dimensional Omics data
• Collaborate with the IT team to establish and maintain the bioinformatics computing and analysis infrastructure
• Develop and execute detailed Omics data generation and analysis plans to support internal program development
• Propose follow-up validation plans and drive cross-functional validation work
• Provide guidance and mentorship to bioinformatics scientists
• Work with research scientists and the global biomarker and translational research team

Associate Director, Bioinformatics

• Accountable for the development and implementation of the regional feasibility strategy
• Collaborate with the global strategic feasibility lead, study teams, and cross-functional stakeholders in the region to deliver strategic feasibility assessments based on comprehensive data analysis
• Provide crucial insights to inform decision-making for effective protocol design and execution
• Conduct and ensure the delivery of high-quality feasibility/site identification assessments
• Evaluate regional capabilities to conduct protocols and achieve targeted enrollment goals
• Act as a liaison between the global strategic feasibility team and region/country
• Assist regional study teams in the successful delivery of allocated feasibility studies
• Ensure adherence to timelines, quality standards, and BeOne's expectations for all studies in scope
• Build expertise within the region regarding Standard of Care, disease landscape, and competitive intelligence
• Stay informed about competing trials, recent or upcoming approvals, prescribing data, insurance claims, and recruitment capabilities

Associate Director, Regional Strategic Feasibility

• Actively influence commercialization strategies that support market planning efforts across BeOne’s oncology portfolio
• Design, execute, and manage market research projects
• Collaborate with cross-functional partners to identify critical business objectives
• Develop and implement market research plans
• Analyze national-level audit data for market sizing and analog assessment
• Integrate primary market research findings with other analytical insights
• Create and implement comprehensive communication plans
• Share key multi-stakeholder insights with partners
• Stay abreast of emerging healthcare and pharmaceutical industry trends

Senior Manager, Global Market Research

• Be exposed to the broad scope of global Regulatory Affairs and specifically CMC Regulatory Affairs and the role’s contribution to drug development and patients’ access to medicines.
• Learn about the role of global Health Authorities in the drug development process.
• Gain hands-on experience in preparing regulatory documents for submission to global health authorities.
• Acquire knowledge about the differences in regulatory requirements across regions.
• Experience CMC technical product development and manufacturing functions in relation to regulatory affairs.
• Responsible for maintaining accurate CMC information in the BeOne Regulatory Information Management system.
• Data remediation.
• Create and maintain CMC Submission Content.
• Upload HA Correspondence/HA Questions/Commitments.
• Maintain internal Regulatory CMC trackers.
• Contribute to Reg CMC process improvements.
• Support the drafting of CTD CMC sections to ensure on-time and high-quality global applications for direct submission to Health Authorities as needed.
• Provide support to Reg CMC team or hiring manager with Regulatory submissions and other tasks as needed.

Intern – Regulatory Affairs, CMC

• Manage, evaluate, and complete regulatory projects
• Develop, implement, and advise on regulatory strategies
• Responsible for managing decision-making and conflict resolution
• Oversee the preparation and submission of documentation
• Liaise and negotiate with regulatory authorities
• Maintain awareness of regulatory environment and assess impact of changes

Senior Manager, Data Steward – AI

Associate Director, Business Analyst – Clinical Operations, Analytics

Senior Manager, Digital Quality Management Systems, Business Analyst

Senior Manager, Healthcare Compliance

Associate Director, Healthcare Compliance

Regional Manager, Hematology

Associate Director, Global Talent Management

Executive Director, Global Commercial Lead

Field Medical Director – Solid Tumor, Breast and Lung

Field Medical Director – Solid Tumor, Breast and Lung

Associate Director, Bioinformatics

Associate Director, Regional Strategic Feasibility

Senior Manager, Global Market Research

Intern – Regulatory Affairs, CMC

Associate Director, Regulatory Affairs