BeOne Medicines

• Responsible for ensuring robust oversight of clinical trial compliance at the country and site level • Apply a risk-based approach to proactively identify, evaluate, and manage compliance risks • Ensure adherence to Good Clinical Practice (GCP), company procedures, and regulatory requirements • Partner closely with country, regional and global stakeholders to safeguard patient safety, data integrity, and inspection readiness • Serve as the primary point of contact for country teams regarding GCP requirements • Analyze and confirm initial country and site-specific risks, communicate trends with Clinical Operations functions • Conduct Site Compliance Visits on identified high risk sites • Support country teams in identifying, managing, and resolving compliance issues

• Ensure robust oversight of clinical trial compliance at the country and site level • Apply a risk-based approach to proactively identify, evaluate, and manage compliance risks • Partner closely with country, regional and global stakeholders to safeguard patient safety, data integrity, and inspection readiness • Serve as the primary point of contact for country teams regarding GCP requirements • Analyze and confirm initial country and site-specific risks • Identify and manage compliance issues, providing support for Corrective and Preventive Actions (CAPAs)

• Promotes BeOne’s Hematology products through calls on targeted physicians in assigned territory • Trains and educates physician support staff on the proper use and handling of BeOne’s Hematology products • Assures healthcare professionals have realistic expectations concerning BeOne’s Hematology products • Maintains communication and integrates activities with BeOne’s Market Access Team • Identifies customer changes and ensures appropriate people and resources are allocated to address the change • Successful completion of all product knowledge coursework • Performs all administrative functions required of the position

• Responsible for ensuring robust oversight of clinical trial compliance at the country and site level • Serve as the primary point of contact for country teams regarding GCP requirements • Analyze and confirm initial country and site-specific risks • Communicate identified country and site trends for continuous improvement • Conduct site compliance visits on identified high-risk sites

• Lead the design and execution of patient journey analytics that identify key moments of intervention, access barriers, treatment transitions, adherence challenges, persistence opportunities, and unmet needs across priority therapeutic areas. • Integrate and analyze longitudinal healthcare data sources, including claims, prescription, specialty pharmacy, EHR, lab, real-world data, clinical trial operations data, market access data, and third-party syndicated datasets. • Develop predictive models and machine learning approaches that support patient identification, biomarker status, provider opportunity assessment, treatment progression, adherence risk, CT acceleration, and engagement prioritization. • Translate model outputs and patient journey findings into clear recommendations, decision frameworks, dashboards, and executive-ready narratives for Commercial, Medical Affairs, and Clinical Operations stakeholders. • Identify practical AI and advanced analytics use cases, including generative AI, natural language interfaces, intelligent automation, and decision intelligence, that improve insight generation and operational effectiveness. • Serve as a subject matter expert for patient journey insights and predictive modeling, helping business, medical, and clinical stakeholders translate strategic questions into analytical approaches, data requirements, and measurable outputs. • Partner with Commercial, Medical Affairs, Clinical Operations, Market Access, Medical Excellence, Clinical Development, Data Engineering, IT, Legal, Privacy, and Compliance teams to ensure analytics solutions are relevant, accurate, scalable, and appropriate for a regulated life sciences environment. • Communicate complex analytical findings in clear, compelling ways through presentations, dashboards, data stories, and decision-support materials for senior stakeholders and cross-functional teams. • Champion responsible AI and model governance practices by promoting transparency, explainability, bias awareness, human oversight, fit-for-purpose validation, and appropriate documentation for AI-enabled decision support. • Lead cross-functional analytics workstreams from problem framing and data assessment through modeling, insight generation, stakeholder review, and implementation support. • Provide technical guidance and mentorship to analysts, data scientists, and external partners to improve analytical rigor, reproducibility, and business relevance. • Establish practical standards, reusable frameworks, and best practices for patient journey analytics, predictive modeling, model monitoring, and insight delivery. • Promote adoption of analytics by increasing stakeholder confidence, building analytics literacy, and embedding insights into commercial planning, medical strategy, evidence generation, and clinical operations execution. • Continuously identify opportunities to modernize tools, data assets, workflows, and AI-enabled processes that improve the speed, quality, and scalability of analytics delivery.

• Ensure end-to-end execution, quality and continuous improvement of global safety operations activities • Oversee effective collection, processing, assessment and reporting of ICSRs against global standards • Oversee safety operations activities in clinical trials, as well as China PV activities • Oversee safety systems and reporting activities • Actively influence GPS’ operational technology strategy • Provide broad and deep technical knowledge • Support and contribute to internal GPS department development • Liaise cross-functionally to execute on PV responsibilities • Create resource requirement projections for safety operations • Recruit, retain, develop, and mentor safety operations staff • Contribute to audits and inspections • Monitor drug safety information communication and ensure timely communication

• Manage biomarker related operational work for clinical trials and programs. • Act as biomarker operation representative to lead/participate in cross-functional activities and initiatives. • Act as key vendor liaison to manage vendor relationship, resolve account level issues and improve processes. • Oversee and manage the performance of junior project managers. • Independently manage biomarker and bio-sample testing activities for clinical trials. • Oversee lab vendor performance and act as key vendor liaison to resolve account level issues and improve collaboration and processes. • Collaborate and communicate with internal functional stakeholders to drive the biomarker related works for clinical trials. • Build collaborative relationships with cross-functional teams as biomarker operation representative and lead/participate cross-functional activities and initiatives. • Collaborate with internal teams to review key study documents and provide training to investigator sites as needed for sample collection schedule, sample processing and shipment. • Participate in clinical study team meetings and program meetings, providing updates and insights related to biomarker activities and progress. • Have a good knowledge of CDx regulations and manage three-way communications with both device partners and lab vendors.

• Accountable for regional study delivery with appropriate inspection-ready quality, within agreed timelines and budget. • Lead the regional clinical operations team and act as point of escalation for issue resolution. • Ensure alignment of regional deliverables with overall study goals. • Collaborate with key stakeholders in the region and provide regular updates on study progress. • Generate, manage, and maintain high-quality study start-up and recruitment timelines for the region. • Ensure timely availability of local adaptations of global study documents and submissions to regulatory authorities. • Work closely with CRAs in the region to ensure proper study execution at sites. • Handle escalated issues or problems with sites in the region. • Monitor regional study activities for compliance with the study protocol, SOPs, and ICH-GCP.

• Participates in the development of global study strategic feasibility proposals in partnership with regional strategic feasibility teams and cross-functional stakeholders • Serves as a feasibility point of contact for assigned studies, programs, or workstreams and liaises cross-functionally • Promotes consistent use of agreed data, tools, templates, and processes across regions • Provides operational feasibility insights to inform study design considerations and optimization discussions • Maintains strong working knowledge of feasibility tools, technologies, databases, and platforms • Supports modelling of strategy options for the study using relevant internal and external data assets • Contributes feasibility insights to strategic planning meetings, training calls, study kick-off meetings, and ongoing study team meetings • Collaborates with Data Science & Operational Excellence, Clinical Systems & Innovation in the development of feasibility tools, systems and platforms • Determines risk/mitigation planning to study feasibility or recruitment and retention of participants • Performs root cause analysis and recommends mitigation steps to address feasibility-related roadblocks

• Responsible for the development, implementation, management, and execution of a coordinated, strategic marketing plan and related tactics, deliverables, and customer-specific access activities. • Align closely with the Market Access field teams in support of current and future indications for BRUKINSA® and TEVIMBRA®. • Develop and advance a keen understanding of overall market access customer needs and create appropriate marketing programs. • Collaborate with BeiGene commercial and medical organization including HEOR, Medical Affairs, Brand Marketing, Legal & Regulatory, and Commercial Operations & Business Analytics teams. • Coalesces field and customer access insights to further refine and advance segment-specific value proposition. • Holds understanding of the complex and evolving market access landscape and challenges, including payer trends and healthcare policy.