BeOne Medicines

Medical writer

• Responsible for writing, editing, and formatting clinical regulatory documents
• Ensure documents conform to regulatory submission and internal document standards
• Collaborate effectively with cross-functional groups
• Manage timelines and communicate with team members
• Review and edit documents authored by others
• Develop and maintain medical writing processes, standards and tools

Senior Medical Writer

Marketing

• Development of product launch and commercialization strategy, driving pre-launch and launch preparations for Oncology portfolio and future pipeline.
• Enhance launch preparations with strong market understanding and knowledge through the development and implementation of relevant marketing tools, analyzing key drivers and barriers and formulating strategic plans to capitalize on market opportunities with close collaboration with the local/regional team and generating extensive insights and analysis.
• Drive the development of cross-functional affiliate marketing plans that identify clear portfolio and brand strategies linked to clearly defined tactical execution.
• Critical to success in this role will be the ability to drive state-of-the-art launches for our future products and the execution of activities to accelerate growth.
• You will be required to facilitate and deliver various activities and training to the affiliate teams to strengthen competencies and onboard new team members.
• Develop and execute marketing end-to-end deliverables and commercialization activities based on stakeholders, disease and brand insights.
• Work closely with supply chain to ensure optimal demand forecast for the portfolio.
• Support the preparation of compelling pricing and timely reimbursement/funding submissions (government funding, tenders and hospital listings) and payor and other stakeholder engagement plans to drive and expand access to BeiGene portfolio.
• Build, where appropriate, value dossiers, objection handlers and payor engagement plans.
• Build and implement patient advocacy plans to enable strong local relations with relevant patient advocacy groups for allocated brands/therapeutic areas.

Marketing and Market Access Manager

Account Manager

• Contribute to BeOne’s sales objective through assigned sales activities
• Provide healthcare professionals with products, services, and information
• Promote BeOne’s Hematology products through targeted physician calls
• Train and educate physician support staff on product use
• Maintain communication with BeOne’s Market Access Team
• Assure realistic expectations for healthcare professionals
• Perform all required administrative functions timely

Account Manager – Hematology

• Promote BeiGene’s Hematology and Solid Tumor products through calls on targeted physicians
• Implement sales, marketing, and patient support programs
• Train and educate physician support staff on product use
• Ensure realistic expectations for healthcare professionals
• Maintain communication and integrate activities with market teams
• Identify customer prescribing trends and territory dynamics
• Complete clinical training and administrative functions
• Communicate insights proactively

Account Manager – Targeted Accounts

Director

• Partner with VP of Market Access to refine, enhance and evolve the market access strategic and tactical plan
• Support the VP Market Access to align the various department segment leaders, provide cross department and cross functional strategic and business insights internally
• Strategic partner to VP of Market Access regarding the identification of industry trends, opportunities, and challenges, providing cross segment, innovative, strategic recommendations and initiatives positioning BeOne as “best in market” market access department
• Lead and operate as the primary contact/liaison for market access regarding cross department collaborations and partnerships
• MA team leader for all new products, market access commercialization planning post early pipeline transition including distribution strategy/planning, department resourcing, reimbursement assessment/planning, National & Strategic accounts, payers and value and access planning
• Access, evaluate, advise, design and implement strategy/operations segment to assist and support the department needs
• Support and partner with VP of Market Access to constantly evaluate department performance and effectiveness, identify opportunities to optimize achieving KPI’s and maximizing results
• Present Market Access strategic updates, landscape assessments, department performances and ad hoc topics/projects to the CLT and leadership team
• Partner with VP of market access to represent and lead segment annual budgeting, tracking spend, revising and enhancing processes and policies
• Triage requests and act as a liaison between the VP of Market Access and other segment leaders and stakeholders to ensure consistent communication and involvement or decision-making at the proper time
• Collaborate with VP and segment leaders in the development of department goals and long-term operational plans
• Listen for and identify connection points and opportunities for agreement across organizations to bring the right stakeholders to the table and drive a coordinated approach
• Anticipate, identify and then facilitate the resolution of issues between departments and across functional lines pertaining to projects, strategic priorities, and team dynamics
• Drive consistent communication and collaboration within the Market Access function and across the organization
• Partner with field team leadership and team members on delivering key messages and identifying gaps and opportunities
• Establish and maintain a work environment that supports learning, respect, open communication, collaboration, integration, and teamwork
• Partner with VP of Market Access to oversee the design, organization and execution of leadership offsite events
• A trusted partner and experienced market access expert

Executive Director, US Market Access Strategy, Evidence & Value

• Oversee daily activities of the Field Medical Team and provide executive-level support for MA leadership
• Maintain and establish credible peer-to-peer scientific relationships with opinion leaders
• Facilitate strategic partnerships with scientific/clinical experts
• Provide feedback/information on emerging clinical and scientific trends
• Prepare field team’s contributions to successful launch and post-launch activities
• Develop and execute regional medical meetings
• Build relationships with internal experts and work cross-functionally

Senior Regional Director – US Field Medical, Breast Cancer

Compliance

• Develop, implement, and advise on NA regulatory strategies for development programs
• Manage NA regulatory aspects of compounds through all phases of development
• Interface with outside regulatory agencies and business partners
• Provide leadership and strategic regulatory oversight for projects
• Review sections of documentation for clinical trials and marketing applications
• Liaise and negotiate with the FDA and Health Canada
• Maintain awareness of global regulatory environment
• Train, develop, and manage an effective regional regulatory team

Director, Regulatory Affairs

Customer Support

• Define and communicate a bold product vision and roadmap that connects BeOne’s mission to measurable patient and caregiver outcomes.
• Lead end-to-end product lifecycle, from strategy and MVP definition through release, learning, and iteration.
• Partner with engineering, UX research, design, marketing, and data science to deliver integrated, scalable experiences.
• Use data, experimentation, and user research to identify friction points and build solutions that deepen engagement and trust.
• Oversee platform integrations across Salesforce, CMS, analytics, and personalization tools, ensuring a unified data ecosystem.
• Establish and monitor KPIs including engagement, satisfaction, performance, accessibility, and conversion.
• Ensure full compliance with HIPAA, GDPR, and WCAG standards while maintaining frictionless user experiences.
• Drive agile execution, sprint planning, and release management across internal and external partners.
• Champion a customer-first culture, balancing measurable impact with empathy, inclusion, and accessibility.

Director, Product Management – Customer Experience, Oncology

• Lead quantitative assessments of pipeline molecules, integrating clinical, commercial, and regulatory factors to evaluate potential success.
• Develop predictive models and scenario analysis frameworks to assess asset progression probability and market access feasibility.
• Utilize claims data and real-world evidence (RWE) to develop Line of Therapy (LoT) models.
• Provide data-driven insights into portfolio prioritization, ensuring BeOne Medicines' R&D investments are aligned with strategic growth objectives.
• Conduct competitive intelligence analyses, tracking industry trends and market opportunities.
• Collaborate cross-functionally with R&D, Commercial, Finance, and Business Development teams.
• Analyze clinical, preclinical, and biomarker data to identify differentiation opportunities.
• Develop valuation models for pipeline molecules, integrating scientific, clinical, regulatory, and market access considerations.
• Support strategic planning for market entry, lifecycle management, and geographic expansion.
• Present findings to senior leadership, distilling complex analyses into clear insights.

Associate Director, Pipeline Analytics

• Manage, evaluate, and complete regulatory projects consistent with company goals
• Lead, develop and implement small molecule CMC regulatory strategies
• Authoring CTD CMC sections for the assigned project to ensure on-time and high-quality global submissions
• Develop regulatory strategy and execute in the preparation of timely responses
• Work collaboratively with cross-functional leads and communicates CMC regulatory strategies
• Lead regulatory risk assessment, identify key CMC regulatory issues
• Provide CMC regulatory review for clinical protocols and investigator brochures for the assigned project

Associate Director, Regulatory CMC – Small Molecule

Medical Director

• Accountable for oversight of benefit/risk safety profile of allocated products through the product lifecycle
• Actively leads and enhances knowledge of safety profiles for allocated products
• Identifies and actively leads management of safety concerns for developmental and approved BeiGene products
• Chairs Safety Management Team (SMT) meetings for assigned products
• Actively leads communication of recommendations to labeling group/other stakeholders
• Leads the review of issue data and closure on recommendations
• Accountable for the content of safety sections of the Development Safety Update Report (DSUR)
• Actively leads safety Issue Assessment and documentation

Executive Medical Director, Product Safety Physician Lead

Business Development Rep

• Develop and maintain forecasts for pipeline assets including assumptions, methodologies, and documentation
• Assess forecast risk and uncertainty, run sensitivities analysis and scenarios
• Conduct primary and secondary market research to understand disease epidemiology, patient segmentation, treatment paradigm, unmet medical needs, competitive landscape, etc.
• Translate insights from market research to both qualitative and quantitative commercial assessment
• Support major planning processes such as LRP, portfolio prioritization and other strategic planning cycles with forecast submissions, scenarios, and narratives
• Coordinate inputs and data from internal sources and external datasets; ensure data quality and consistent use of definitions/assumptions across teams
• Provide commercial/business case assessment to inform pipeline programs’ go-no-go and critical investment decisions
• Collaborate with cross-functional teams to establish Target Product Profiles and develop market positioning strategies for early-stage pipeline programs
• Collaborate with cross-functional teams to establish relevant Disease Area Strategies

Associate Director, Pipeline and Business Development Valuation

Project Manager

• Translate, implement, and advise on global regulatory strategies for development programs
• Act as a key advisor to the GRL/RRL, providing strategic regulatory oversight and recommendations for global product development, submissions, and lifecycle management
• Lead and manage complex regulatory submissions (IND/CTA, NDA/BLA/MAA) across multiple regions, ensuring compliance with ICH, US, EU, China, and other international requirements
• Organize and facilitate cross-functional meetings with global teams to coordinate, plan, and track submission activities
• Proactively identify risks, propose solutions, and manage critical issues related to global regulatory submissions and strategy
• Oversee preparation and submission of documentation to support investigational and marketing registration packages
• Build partnerships with senior stakeholders and cross-functional teams (clinical, medical, safety, CMC, commercial) across regions
• Mentor and guide junior staff in project planning, regulatory processes, and professional development
• Champion process optimization and improvement initiatives within the global regulatory PM function

Associate Director – Global Regulatory Project Management

• Support, translate, and implement global regulatory strategies for development programs.
• Serve as a principal advisor to the Global Regulatory Lead.
• Maintain awareness of global regulatory environments.
• Lead and manage complex regulatory submissions across multiple regions.
• Act as the “COO” to the Global Regulatory Lead.
• Organize and facilitate cross-functional meetings.
• Proactively identify risks related to global regulatory submissions.
• Mentor, guide, and develop junior and mid-level staff.

Director, Global Regulatory Project Management

Clinical Operations

• Lead the end-to-end global budget & resource management/utilization within GCO
• Develop and implement global budget and resource planning/management strategy for GCO
• Build, maintain & optimize best-in-class integrated Resource Budgeting, Resource Allocation & Resource Management models
• Establish & manage a centralized process and governance model for tracking, forecasting, and reporting Opex and workforce targets, allocation and utilization
• Serve as a strategic advisor to the GCO leadership team on resource-related decisions
• Generate analytics & insights relating to portfolio demand as well as resource availability/utilization