BeOne Medicines

Director

• Facilitate generation of, author, update, and/or review key documents, including, but not limited to: Protocol concepts, synopses, protocols, and amendments; Informed consent documents; Investigator Brochures; Clinical study reports; Abstracts, posters and manuscripts; Clinical sections of INDs (and equivalent applications), NDAs (and equivalent applications), Annual Reports, and Developmental Safety Update Reports; Clinical sections of Health Authority Briefing Documents, Orphan Drug applications, and annual reports; Risks / benefits analysis for applicable documents; Clinical Development Plans.
• Partner with clinical operations and other functional areas for the successful implementation and execution of clinical studies.
• Provide scientific expertise for selection of investigator and vendors.
• Train BeOne colleagues, CRO staff, and study site staff on the therapeutic area, molecule, and/or clinical protocol.
• Provide scientific and medical support throughout conduct of a clinical trial; respond to clinical questions from sites, IRBs/IECs, Health Authorities, and CRO’s.
• Review, query, and analyze clinical trial data.
• Interpret, and present clinical trial data both internally and externally.
• Represent a clinical study or development program on one or more teams or subteams.
• Create clinical study or program-related slide decks for internal and external use.
• Build and maintain opinion leader/investigator networks; organize and present at key opinion leader advisory boards and investigator meetings.
• Contribute to or perform therapeutic area/indication research and competitor analysis.
• Build strong relationships with internal experts.
• Identify continuous process improvement opportunities.
• Identify incremental organizational resource needs – staff, budget, and systems.
• Develop, track, execute and report on goals and objectives.
• Support budget planning and management.
• Be accountable for compliant business practices.

Director, Clinical Development – Biotech Unit

• Defines operational strategy for assigned clinical programs and translates it into concrete steps for operational implementation.
• Builds long term indication level operational plans, in collaboration with regional and country stakeholders.
• Drives Program strategy and indication knowledge in team and adapts operations accordingly.
• Ensures that knowledge of the global marketplace and competitors is used within assigned program to create operational competitive strategies and plans and defines objectives around emerging patient needs.
• Ensures consolidation, oversight, and forecast of key trial conduct milestones.
• Liaises with other program Regional Program Leads and Regional Feasibility Leads during feasibility for overlapping or synergistic indications/populations across programs.
• Provides leadership to the Regional Clinical Study Managers for the delivery of one or several clinical trials in the region, within timelines, budget and appropriate inspection readiness quality.
• Is responsible for the country selection on the studies of their program in collaboration with the Regional Clinical Study Manager and based on feasibility conducted by country teams and the Regional Strategic Feasibility Lead.
• Represents the region in discussions at Global Program Level and Governance boards (GCPL, DCT, GPT, bi-weekly business review meetings).

Associate Director – Regional Program Lead

Account Manager

• Territory to cover: South West England & South Wales
• Development and execution of strong regional plans with cross-functional support.
• Using expertise in haem-oncology be a go-to scientific and patient care resource for stakeholders in the assigned region.
• Collaborate with health system partners, health care practitioners (HCP), regional patient advocacy groups, and relevant stakeholder groups in the region.
• Build BeOne image/brand and awareness for the company and products in the haematology-oncology market.
• Plan, identify, analyse, and implement activities and meetings to optimise regional potential.
• Ensure that the target customers are updated on product strategy and communication.
• Collaborate with regional Key Opinion Leaders, Head of Clinics and Expert/Therapy group members.
• Provide scientific expert advice and support for opinion leaders and medical haemato-oncologists in hospitals and private clinics.
• Responsibility for the regional sales goals and qualitative performance parameters.
• Development, implementation, and execution of projects to optimize patient care in collaboration with key customers.
• Organise and execute local symposia, educations and workshops with key customers.
• Ensure compliance within all activities to maintain the highest standards of patient-focused ethical conduct in line with BeOne´s standards.

Key Account Manager

Clinical Research

• Accountable for regional study delivery with appropriate inspection readiness quality, within agreed timelines and budget
• Leads the regional clinical operations team and acts as point of escalation for resolution of issues
• Ensures alignment of regional deliverables with overall study goals
• Collaborates with key stakeholders in the region and provides regular updates on study progress to senior management
• Reviews and signs-off monitoring reports
• Prepares sites for quality assurance audits and inspections

Regional Clinical Study Manager

Clinical Operations

• Lead the strategic planning and execution of study start-up activities across clinical programs, ensuring rapid, high-quality site activation.
• Provide leadership to cross-functional teams, oversee budgets, engage key stakeholders, and drive continuous process improvements.
• Develop and implement activation strategies, manage regulatory and ethics submissions (IRB/EC and Health Authorities), oversee site contract and budget negotiations.
• Monitor operational KPIs, ensure audit and inspection readiness, and lead end-to-end study start-up activities.
• Drive continuous improvement initiatives focused on reducing activation timelines and increasing predictability, and evaluate and introduce innovative tools.
• Champion change management related to new systems, SOPs, and operational models.

Senior Director, Global Clinical Operations, Study Start-Up

Marketing

• Serve as the primary Brand Champion ensuring strategy development and tactical execution across all internal stakeholders
• Oversee the development and execution of the brand vision, positioning, strategy and messaging to address market landscape dynamics across indications
• Core member of the Global Brand Team (GBT) to ensure line of sight and US commercial POV representation
• Partner cross-functionally with Sales, Medical Affairs, Market Access, HEOR, Finance, Corporate Affairs and Advocacy, Government Affairs, and other functions as needed to align strategy, messaging, data generation and publication priorities, and tactical planning and execution that will maximize brand value
• Lead the development of the patient strategy and tactical plan in alignment with the overall brand strategy across channels (web, video/TV, and social media) that will enhance brand performance
• Collaborate with Global Insights & Analytics to initiate and analyze market data and primary research and leverage regional marketing team KOL insights to assess customer needs and the competitive landscape to inform strategic decisions for the brand
• Anticipate and establish scenario plans for different outcomes and changes in the competitive landscape, unmet need, access scenarios, strategic implications and action plans, including development and ongoing optimization of forward looking brand messaging based on publication and strategic planning
• Lead annual strategic planning processes for the brand (Brand Plan, LRP, AOP), including net revenue forecast development with the support of Global Insights & Analytics, OPEX investment planning, and P&L planning
• Ensure net revenue forecast attainment, OPEX management, investment trade-off analysis, and P&L attainment quarterly and annually consistent with Brand Plan, LRP, and AOP
• Lead quarterly business reviews in coordination with the Insights & Analytics and Finance teams
• Develop measurement plans to assess effectiveness of initiatives using advanced analytics in collaboration with the Insights & Analytics and Omnichannel teams
• Collaborate with Sales Leadership, Commercial Learning and Development, and Market Access on field execution of marketing strategy and messaging using PRC-approved materials (marketing materials, reprints, FAQs, FDMs, etc.)
• Ensure compliance with all Legal, Regulatory, Privacy, and Pharmacovigilance requirements
• Establish clear goals and align team efforts with business objectives and priorities
• Foster collaboration, accountability, and professional development within the team.

Senior Director – Hematology Marketing Brand Lead

Medical Director

• Support BeOne 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
• Serve as an internal resource of clinical and scientific information
• Nominate sites to Clinical Operations to participate in clinical research
• Assist in the development and execution of clinically relevant regional medical meetings
• Support Medical Affairs budget planning and management

Senior Field Medical Director, Hematology - Gulf States Territory

• Lead development, enhancement, and execution of national short‑ and long‑range forecast models for U.S. Hematology assets.
• Integrate insights from primary research, secondary data, claims analytics, and competitive intelligence into forecast assumptions.
• Partner with Pipeline teams to build forecast inputs for future indications and incorporate them into long‑range forecasting frameworks.
• Manage ad‑hoc analytics to support strategic decision‑making, synthesizing diverse data sources into actionable insights.
• Provide clear communication to Senior Leadership on forecast expectations, risks, opportunities, and key business drivers.
• Lead, mentor, and develop a high‑performing team with strong technical and strategic capabilities.
• Collaborate with Marketing, Sales, Finance, Market Access, Supply Chain, and Medical to ensure alignment on performance expectations and strategic planning.

Director, Forecasting and Analytics

• Collaborate with lead project Biostatician in project strategic planning and provide overall guidance to the programming team in creation, implementation, and maintenance of programming development plans for each project accounting for timelines, resources, and quality deliverables for all project work assigned; ensure that all programming has been carried out per industry and internal standard practice.
• Represent the statistical programming team at Study Management Team and Clinical Development meetings to address deliverables and timelines
• Contribute to the development and implementation of programming resource algorithms.
• Collaborate with programming managers and project leads, lead the effort of project resource planning and tracking.
• Interact and communicate with Statisticians, Data Managers, Clinical Operations, Medical Monitors, Medical Writing and Medical Monitors to address programming related study deliverables
• Contribute to strategies for programming related matters in submission to regulatory agencies, publications and other communications as needed
• Understand and execute department-, product- and study-level macros and utilities.
• Write, test and validate product- and study-level macros and utilities
• Be a technical resource for programming groups to provide advice on complex programming tasks and/or standards.
• Assist in the review of key study-related documents produced by other functions, e.g. SAP, case report form, data management plan, database specifications, EDC data structures, DMC plans and other clinical documents
• Oversee the projects for the creation of analysis datasets, production / validation of output, and review of annotated case report forms
• Lead the statistical programming support of FDA/EMEA/CDE regulatory submissions follow CDISC standards
• Contribute to departmental process and standards initiatives such as tools and CDISC standards.
• Collaborate and support the selection and management of CROs (including the strategic outsourcing providers) conducting statistical programming.
• Oversee the work in support of clinical trials, ad-hoc analysis requests, data validation, etc. in accordance with all relevant statistical regulatory guidance and standards.
• Lead the development of TAUG (therapeutic area users guide) following CDISC Industry standards

Associate Director, Scientific Programming

Compliance

• Develop and implement global regulatory strategies for development programs
• Manage regulatory aspects of compounds through all phases of development
• Provide leadership and strategic regulatory oversight for designated projects
• Interface with business partners regarding global development, regulatory, and registration strategies
• Support preparation and submission of global regulatory documentation

Director, Global Regulatory Lead

Medical writer

• Provide expertise to support the development of clinical and regulatory documents
• Mentor junior MWs as needed
• Manage multiple documents including complex ones
• Collaborate with study teams for document development
• Create and maintain document writing templates and guidance
• Identify potential risks and make mitigation plans
• Provide technical mentorship to junior MWs
• Share regulatory writing knowledge across teams

Principal Medical Writer

Research Analyst

• Complete appropriate therapeutic, protocol and clinical research training/CRA training to perform job duties.
• Perform site selection and evaluation, supporting initial list of sites and recruitment targets.
• Conduct onsite/remote pre-study, initiation, routine monitoring and closeout visits per monitoring plan.
• Create and maintain documentation regarding site management and monitoring visit findings.
• Ensure inspection readiness of the study and sites.
• Collaborate with Country and Regional Clinical Study Managers to ensure timely delivery of study milestones.
• Mentor junior staff (Associate CRA and CRA) and act as the escalation point person for CRA(s) with site-related issues.

Senior Clinical Research Associate

Administrative Assistant

• Provide support to various teams within BeiGene.
• Coordinate meetings and events.
• Manage office equipment and supplies.
• Handle payments, finances, and expense monitoring.
• Track the annual budget with attention to departmental allocations.
• Liaise with vendors and manage the onboarding process.
• Assist with travel arrangements for senior members.
• Conduct clerical duties including filing and preparing documents.

Senior Administrative Assistant

Manager

• Design and develop new integrations within Workday across various modules including Core HCM, Payroll, Recruiting, and Onboarding, ensuring alignment with organizational needs and best practices.
• Provide ongoing maintenance and support for existing inbound and outbound integrations with vendors such as payroll providers, benefits carriers, finance, identity management, and third-party HCM.
• Actively monitor integration processes, troubleshoot and resolve integration failures, performance issues, and data discrepancies to ensure operational stability.
• Configure and manage Workday security for integrations, including domains, business process security policies, and integration system user permissions (ISU and ISSGs).
• Create and maintain comprehensive documentation for integrations including technical specifications, process flows, test scripts and user guides to support ongoing projects and team knowledge.
• Perform unit testing, system integration testing (SIT), and support UAT to ensure new and updated integrations meet functional and performance standards.
• Leverage REST/SOAP APIs, OAuth, and JSON to connect Workday with external systems.
• Create Complex Calc fields and advanced custom reports within workday to streamline integration processes and optimize data flow.
• Assist in audit and compliance activities by providing required documentation and evidence where necessary.
• Ensure compliance with data privacy regulations (SOX, GDPR where applicable).
• Collaborate with cross-functional stakeholders to gather requirements for new enhancements and modifications to existing integrations, aligning with business goals.
• Identify and recommend process improvements and system enhancements to support business strategies and operational needs.
• Keep abreast of Workday updates and new features related to integrations, evaluating their potential impact on current processes and recommending enhancements as applicable.
• Actively engage in technical discussions and integration-related activities, including but not limited to release management, troubleshooting and ad-hoc projects.

Manager – Workday Integrations

• Contribute to BeiGene’s overall sales objective by performing assigned sales activities
• Promote BeiGene’s Solid Tumor products through calls on targeted physicians in assigned territory
• Train and educate physician support staff
• Maintain communication and integrate activities with Market Access, Field Reimbursement, and Contract Account Teams
• Identify customer changes and ensure coordinated communication and planning
• Perform all administrative functions, including reporting call activity and customer information
• Assist in the identification and resolution of issues and communicate proactively

Account Manager – Solid Tumor

• Accountable and responsible for building, developing and retaining the global team of gCSM
• Oversee the delivery and goal achievement of projects within the designated program(s)
• Collaborate with GCPLs to define and implement strategies and key priorities across-programs
• Provide clinical operational insight to drive the program strategy
• Conduct regular program review meetings to mentor, support, and ensure all studies are tracking to the DCT/DRC-approved budget and timeline

Director, GCO Program Lead

• Lead the Central Statistical Monitoring (CSM) team within the Global Statistics department
• Support the RBQM: providing statistical design, interpretation, and governance for monitoring activities
• Accountable for development, validation, and operationalization of statistical monitoring indicators and models
• Acts as the CSM statistician interfacing with clinical study statisticians, medical monitors, safety/pharmacovigilance, global clinical operations (GCO), quality/GCP, data management
• Defines statistical thresholds, signal characterization methods, and recommended investigative workflows
• Escalates safety or major data integrity concerns to medical monitors, safety leadership, and quality
• Develop and maintain statistical risk indicators (KRIs), anomaly detection methods, and monitoring tools
• Validate models and algorithms: assumptions, diagnostics, false positive/negative rates, sensitivity analyses, and reproducibility
• Implement processes to detect candidate signals across sites, subjects, and data domains
• Develop and deliver training modules for clinical monitors

Director, Biostatistician – Evergreen

• Responsible for maximizing BeOne's products in the served territory
• Develop territory specific strategic account plans
• Supports and advises the key account customers in an appreciative, open minded and honest manner
• Building a BeOne image/brand and awareness for our company and our products in the oncology market
• Develop long lasting relationships based on value addition to the key stakeholders of the assigned territory
• Responsibility for regional sales, company reputation, access goals and qualitative performance parameters
• Development, implementation and execution of commercial projects to optimize patient care
• Organization and execution of local symposia and workshops with the key customers
• Gathering insights and analyzing available information to identify strategic opportunities at account level
• Participation and customer care in local, national and international meetings and symposia
• Ensure compliance within all activities to maintain the highest standards of patients focused ethical conduct

Key Account Manager – Solid Tumors

• Support the design, development, and continuous improvement of the clinical trial costing tool
• Support the development and refine costing models and algorithms for Phase I–III clinical trials, incorporating functional inputs across global clinical operations
• Ensure cost drivers, assumptions, effort models, service levels, and resource seniority levels are accurate
• Partner with functional subject matter experts (SMEs) to maintain up-to-date operational parameters and cost benchmarks
• Support the leadership in implementing and overseeing the cross-functional governance frameworks
• Develop standard operating procedures (SOPs), guidance documents, and training materials
• Work closely with Resource Management to integrate capacity, utilization, and effort drivers into costing models
• Collaborate with Finance on resource structure, budget methodologies and validation processes
• Guide integration of the costing tool with enterprise systems