BeOne Medicines

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

Account Manager

• 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

Director

• 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

Clinical Research

• 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

Senior Manager, Clinical Costing and Pricing

Compliance

• Serve as a trusted, strategic advisor to Global R&D stakeholders, providing real-time, practical compliance guidance.
• Maintain advanced knowledge of laws, regulations, and industry codes applicable to R&D.
• Oversee the development, implementation, and maintenance of Global R&D compliance policies and related SOPs.
• Design, deliver, and evaluate engaging, role-based compliance training for R&D stakeholders.
• Conduct live and remote monitoring of R&D activities and provide timely feedback to stakeholders.
• Ensure interactions with HCPs, HCOs, study subjects, and community groups comply with BeOne policies and industry standards.

Director, Global R&D Compliance

Medical Director

• Support BeOne clinical assets and pipeline by successful execution of clinical development programs and deliverables in partnership across the organization, with external vendors, and with external academicians and collaboration partners.
• Assess and execute clinical programs and help assure that activities are executed within expected scope, budget and timelines.
• Establish and grow Clinical Research functions to assure best-in-class global capabilities and execution.
• Work closely with colleagues in clinical development, program management, biometrics, clinical operations, safety/pharmacovigilance, regulatory, molecular diagnostics, and translational research and other functions.
• Facilitate generation of key documents, including protocols, informed consent documents, Investigator Brochures, clinical study reports, and more.
• Partner with clinical operations and other functional areas for successful implementation and execution of clinical studies.
• Provide scientific expertise for selection of investigator and vendors.
• Train BeOne colleagues, study site staff on the therapeutic area, molecule, and/or clinical protocol.
• Review, query, and analyze clinical trial data; interpret, and present clinical trial data both internally and externally.

Medical Director, Hematology

• Promote BeOne’s Hematology products through calls on targeted physicians
• Train and educate physician support staff
• Assure healthcare professionals have realistic expectations
• Maintain communication with BeOne’s Market Access Team
• Identify customer changes and ensure appropriate resources are allocated
• Complete product knowledge coursework and LMS/Compliance Wire assignments
• Perform all administrative functions necessary for the position
• Assist in identifying and resolving issues

Account Manager – Hematology

Clinical Operations

• Lead and execute the organizational change management strategy for Global Clinical Operations learning and development initiatives
• Drive end to end change management for complex, cross functional, and global clinical operations process changes
• Partner with Global and Regional Clinical Operations leaders and learning business partners to support implementation of new processes, systems, and ways of working
• Develop and execute integrated change, communication, and hyper care plans to support operational readiness, adoption, and sustained behavior change
• Identify and manage risks, resistance, and adoption barriers
• Monitor and assess change effectiveness through defined metrics, feedback, and performance indicators
• Support continuous improvement by capturing lessons learned and embedding change management best practices

Associate Director, Change Management, Global Clinical Operations – Learning and Development

• BeiGene is seeking an experienced Senior IT Audit Manager to join our growing internal audit (IA) function
• Responsible for IA assurance activities from a business, technology, and security perspective across the organization
• Support the achievement of the Company’s business objectives
• Engage in the risk assessment process by identifying and evaluating technology-related risks
• Implement and maintain risk management strategies for Internal Audit
• Lead complex and/or global financial, compliance, and operational audits
• Develop risk-based, tailored audit programs across a wide variety of IT risks
• Conduct on-site fieldwork to assess the Company’s information system and security related processes and controls
• Ensure all audit program steps are completed

Senior Manager, IT Audit

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.
• Present and defend commercial cases in front of senior leadership.
• 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.