The individual is responsible for developing and executing patient support programs, educational initiatives, and promotional strategies to drive the growth of oncology products. They will lead cross-functional collaboration and manage the end-to-end lifecycle of promotional materials while monitoring program performance.
The Senior Medical Director will lead clinical development programs for hematology assets, overseeing strategy, execution, and cross-functional collaboration. They are responsible for authoring key clinical documents, managing investigator networks, and ensuring compliance with global regulatory standards.
The Associate Director leads the planning, coordination, and execution of global medical initiatives and integrated evidence plans for the hematology franchise. They also drive continuous improvement within the PMO by implementing standardized processes and performance metrics across Global Medical Affairs.
The associate is responsible for developing accurate and compliant investigator site budgets to facilitate financial planning and fair market value negotiations. They also perform budget variance analysis, scenario modeling, and provide strategic insights to support clinical trial financial forecasting.
The Associate Director leads and executes global regulatory strategies across the drug development lifecycle, ensuring alignment with business objectives. They manage complex regulatory submissions and coordinate cross-functional teams to secure market access worldwide.
The Field Medical Director will develop regional strategies to support pre-clinical and clinical pipeline development for solid tumor assets. They will establish peer-to-peer scientific relationships with opinion leaders and facilitate strategic partnerships with clinical experts.
Lead program management for oncology drug development and product lifecycle management while driving strategic team decision-making. Facilitate alignment across key functions and stakeholders to ensure the successful delivery of global asset development strategies.
The Executive Director will lead and oversee the execution of Global Medical Affairs plans for solid tumors, including gynecologic cancer programs. They will represent Medical Affairs in clinical development teams, manage data generation strategies, and build relationships with key opinion leaders globally.
The specialist manages clinical drug supply activities, including planning, label development, and distribution to ensure continuous supply for clinical trials. They collaborate with internal and external stakeholders to develop supply strategies, monitor production schedules, and oversee IRT system activities.
The Director will lead the strategic planning, performance measurement, and AI enablement initiatives for the global Corporate Affairs function. They will partner with leadership to translate strategy into execution, drive organizational alignment, and build scalable data-driven capabilities.
The Financial Analyst will provide tactical financial support for global enabling functions by tracking departmental spending and managing key processes like PO approvals and monthly reporting. They will also perform variance analysis, support annual budgeting cycles, and provide actionable insights to leadership for decision-making.
The Senior Field Contracting Manager is responsible for the strategic execution of institutional contracting and securing product access across hematology and oncology accounts. This role involves leading negotiations with hospital buying groups and procurement bodies while aligning pricing strategies with local institutional realities.
The Senior Director is responsible for developing and implementing global regulatory strategies for oncology development programs to ensure market access. They will manage regulatory aspects of assets throughout the product lifecycle and provide strategic oversight for clinical studies conducted on the company's Clinical SuperHighway.
The Senior Director is responsible for developing clinical program strategies and ensuring the successful execution of partnership programs within the Global Development SuperHighway. They provide scientific leadership, oversee clinical trial data, and manage cross-functional teams to meet regulatory and commercial objectives.
The Senior Manager will plan and manage regulatory activities, including the preparation and submission of regulatory dossiers such as INDs and BLAs. They will also provide regulatory strategy guidance to cross-functional project teams and ensure ongoing compliance with global regulatory requirements.
The Analytical Technical Lead serves as the global point of contact for analytical lifecycle management of commercial small molecule products. This role ensures robust analytical control strategies, manages regulatory compliance, and oversees quality investigations across internal and external networks.
The Senior Global Clinical Study Manager is responsible for leading global cross-functional study teams to ensure the efficient delivery of clinical trials within budget and timelines. They oversee external partners, manage study-related risks, and ensure high-quality execution and inspection readiness throughout the study lifecycle.
The GCO Program Lead is responsible for the strategic operational planning and clinical execution of designated oncology programs. This role involves leading global clinical study managers, managing program budgets, and collaborating cross-functionally to ensure high-quality delivery of clinical trials.
The role leads global clinical process management activities to ensure processes are efficient, compliant, and aligned with regulatory standards. It serves as a key liaison between regional heads and cross-functional partners while mentoring staff to support capability development.
The Senior Director leads the global strategy, governance, and operational execution of clinical site contracting to ensure rapid study startup and compliance. They manage a global team while collaborating with cross-functional stakeholders to optimize processes and drive operational excellence.
The role serves as a technical lead and project manager for statistical programming deliverables across multiple clinical studies. Responsibilities include managing study timelines, collaborating with cross-functional teams, and ensuring high-quality programming outputs for regulatory submissions.
The Regional Clinical Study Manager is responsible for leading regional clinical operations, ensuring study delivery within timelines and budget, and maintaining inspection readiness. They act as the primary point of escalation for regional issues and collaborate with global teams and external vendors to ensure study goals are met.
The Key Account Manager is responsible for maximizing product sales within the assigned territory by implementing marketing strategies and achieving defined sales targets. They also provide expert scientific support to hospital pharmacists and oncologists while managing commercial projects to optimize patient care.
The Senior Contract Associate is responsible for drafting, negotiating, and finalizing complex clinical site contracts and budgets for clinical trials. They serve as the primary point of contact between internal departments and external sites to ensure all agreements are executed in compliance with regulatory requirements and project timelines.
The Lead is accountable for the lifecycle management of drug development and commercialization within the partnership program, driving strategic team decision-making and delivery of goals. They are responsible for developing project plans, managing operational KPIs, and fostering collaboration across internal and external teams to ensure high-quality execution.
The Executive Director will lead global operational strategy, financial stewardship, and compliance initiatives across the Clinical Business Operations team. They are responsible for overseeing investigator budgets, site contracts, site payments, and workforce planning to ensure operational excellence and data integrity.
The Senior Manager is responsible for managing and executing a risk-based audit program for GxP computerized systems to ensure compliance throughout their lifecycle. This role involves leading internal and third-party audits, assessing compliance risks, and driving sustainable corrective and preventive actions.
The Marketing Lead is responsible for developing and implementing go-to-market strategies to maximize product performance in the German hematology market. They will lead cross-functional collaboration to create brand plans, manage promotional materials, and ensure commercial targets are met.
The Senior Medical Director serves as the Lead Product Safety Physician for complex developmental programs, overseeing the benefit/risk safety profile throughout the product life cycle. They are responsible for managing safety concerns, leading safety management teams, and ensuring regulatory compliance through effective communication and data analysis.
The Senior Specialist independently manages the triage, case processing, and quality control of individual case safety reports to ensure regulatory compliance. They also perform SAE reconciliation between safety and clinical databases while meeting quality and productivity metrics.
The Manager, Global ICSR Management oversees triage, case processing, and quality control to ensure compliance and efficiency in safety reporting. They also lead cross-functional projects, manage SAE reconciliation, and drive continuous improvement initiatives within the safety operations team.
The Senior Contract Associate is responsible for drafting, negotiating, and finalizing complex clinical site contracts and budgets throughout the study lifecycle. They serve as the primary point of contact between internal departments and external sites to ensure compliance and timely execution of agreements.
The Associate Director will influence commercialization strategies by designing and executing primary market research projects for the oncology pipeline. They will collaborate with cross-functional teams to translate research findings into actionable insights that support data-driven decision-making.
The Regional Clinical Study Manager is accountable for regional study delivery, ensuring quality, inspection readiness, and adherence to timelines and budgets. They lead the regional clinical operations team, manage external vendors, and act as the primary point of escalation for study-related issues.
The Director of Digital Solution Architecture defines and governs the global commercial technology ecosystem, including CRM, omnichannel engagement, and data integration platforms. They act as a strategic advisor to leadership to drive technology investment, innovation, and digital transformation across commercial and medical functions.
The Senior Director will lead global tax strategy, including complex cross-border planning, transfer pricing, and tax-efficient structuring for R&D and commercial operations. They will also manage tax risk, ensure compliance with evolving global regulations, and provide clear tax insights to senior leadership and the Board.
The Executive Director oversees global tax reporting, compliance governance, and tax technology modernization while serving as a strategic advisor to Finance leadership. This role drives continuous improvement, automation, and AI adoption across the global tax function to support the company's growth objectives.
The Senior Director will lead clinical, health economics, and outcomes research communications to inform population health decision-makers about product value. They will build peer-to-peer relationships with payers and provide strategic leadership on HEOR projects and market access activities.
The Study Start-up Specialist is responsible for managing local start-up activities, including regulatory submissions, budget negotiations, and site documentation. They collaborate with clinical teams to ensure study timelines are met while maintaining quality standards and inspection readiness.
The Senior Director is responsible for the strategic operational planning and clinical performance of the Hematology franchise, including managing the Global Clinical Program Lead and Study Manager groups. They act as a key representative for clinical operations, driving therapeutic strategy and ensuring execution excellence across global clinical programs.
The Sales Representative will manage and develop relationships with key accounts, including wholesalers and payers, while implementing effective negotiation strategies. They are responsible for promoting specialized therapeutic products and maintaining accurate records within the company's CRM system.
The Senior Manager will apply advanced analytics and statistical methods to strengthen quality oversight of clinical development, patient safety, and regulated research. They will develop and maintain analytical tools and dashboards to identify emerging risks and support evidence-based decision-making across the R&D portfolio.
The Clinical Research Associate executes clinical monitoring activities at trial sites in accordance with ICH-GCP guidelines and local regulations. They are responsible for site selection, initiation, recruitment oversight, and ensuring data quality throughout the lifecycle of oncology and hematology clinical trials.
The specialist is responsible for managing study start-up activities in Germany and Austria, including regulatory submissions and site performance tracking. They collaborate with clinical study managers to ensure adherence to timelines, quality standards, and GCP requirements.
The Regional Clinical Study Manager is accountable for regional study delivery, ensuring quality, inspection readiness, and adherence to timelines and budgets. They lead the regional clinical operations team, manage external vendors, and collaborate with key stakeholders to ensure successful trial execution.
The Regional Clinical Study Manager is accountable for regional study delivery, ensuring quality, inspection readiness, and adherence to timelines and budgets. They lead the regional clinical operations team, manage external vendors, and act as the primary point of escalation for study-related issues.
The Regional Clinical Study Manager is accountable for regional study delivery, ensuring quality, inspection readiness, and adherence to timelines and budgets. They lead the regional clinical operations team, manage external vendors, and act as the primary point of escalation for study-related issues.
The Clinical Research Manager acts as a line manager for trial monitoring staff, overseeing their performance, training, and professional development. They are responsible for managing study start-up activities, ensuring adherence to ICH/GCP guidelines, and collaborating with regional operations to meet study timelines and quality standards.
The role involves line managing clinical study managers, overseeing their performance, and ensuring clinical trials are executed according to ICH/GCP guidelines and corporate standards. The manager will also drive process improvements, allocate resources, and provide local expertise to support clinical trial activities.
The Clinical Research Associate executes clinical monitoring activities at trial sites in accordance with ICH-GCP guidelines and local regulations. They are responsible for site management, recruitment tracking, data quality assurance, and collaborating with the Regional Clinical Operations Manager to ensure study timelines are met.
The Senior CRA is responsible for conducting clinical site visits, ensuring protocol compliance, and maintaining effective relationships with site personnel. They also monitor data quality, patient safety, and provide training to site staff while mentoring less experienced team members.
The Director will lead the design, innovation, and scaling of omnichannel engagement capabilities across Global Medical Affairs to create connected, customer-centered experiences. This role involves translating medical strategy and customer insights into coordinated engagement plans while establishing frameworks and playbooks for consistent execution.
The Associate Director provides leadership and line management to Global Study Management Associates, ensuring high-quality study delivery and operational excellence. They are responsible for resource allocation, process optimization, and driving strategic initiatives across clinical study portfolios.
The Senior Manager will apply advanced analytics and statistical methods to strengthen quality oversight of clinical development and patient safety. They will develop predictive risk models and dashboards to identify systemic risks and support evidence-based decision-making across regulated R&D activities.
The Director will own the end-to-end system management lifecycle for all external Global Clinical Operations applications and platforms. They are responsible for driving system maintenance, ensuring data integrity and security, and collaborating with stakeholders to align technology investments with organizational goals.
Lead the development and implementation of clinical operations excellence strategies, ensuring GCP compliance and quality across global clinical trials. Manage cross-functional teams and processes, including eTMF oversight, performance metrics, and continuous improvement initiatives.
The role is responsible for driving operational excellence and process optimization within the Program and Study Management function. It involves leading strategic initiatives, managing cross-functional collaborations, and ensuring clinical studies are executed efficiently and in compliance with regulatory standards.
The Senior Medical Science Liaison is responsible for building professional relationships with healthcare professionals and key opinion leaders to exchange scientific information. They also collect medical insights, support clinical trials, and contribute to the execution of medical affairs strategies within the assigned region.
The Contract Manager oversees the planning, drafting, and negotiation of clinical site contracts to ensure compliance with legal and regulatory requirements. They also provide functional line management to contract associates and serve as a key point of contact for clinical operations and legal teams.
The GCO Program Lead is responsible for the strategic operational planning and clinical execution of designated programs while providing leadership to global clinical study managers. They act as a key point of escalation for issue resolution and collaborate with cross-functional teams to drive disease and asset strategy.
Supports the Global Clinical Study Manager in the delivery of global clinical studies by ensuring quality standards, timelines, and budget adherence. Manages study-level documentation, system setups, and cross-functional team coordination to facilitate efficient clinical trial execution.
The Director of Comparator Sourcing defines and executes global sourcing strategies to ensure reliable access to comparator medicines for clinical development. This role leads a global team, manages supplier partnerships, and drives cross-functional initiatives to optimize supply chain performance and compliance.
The Field Medical Director will develop regional strategies to support pre-clinical and clinical pipeline development while fostering relationships with key opinion leaders and healthcare providers. They will also serve as a cross-functional liaison to ensure scientific alignment across medical affairs, clinical development, and commercial teams.
The Director, Safety Scientist leads the detection, evaluation, and management of safety signals for assigned compounds while ensuring compliance with global regulatory requirements. They provide clinical and scientific expertise to cross-functional teams and represent the safety department in regulatory interactions and governance meetings.
The R&D Sourcer focuses on talent sourcing, pipelining, and intelligence to build candidate slates for critical R&D roles. They act as a talent advisor providing market insights and competitive intelligence to business leaders and recruiters.
Accountable for regional clinical study delivery, managing regional operations teams and external vendors to ensure timelines and budgets are met. Responsible for ensuring inspection readiness, regulatory compliance, and alignment of regional deliverables with global study goals.
Develop and execute the patient advocacy strategy for Germany to build lasting partnerships with patient organizations. Ensure the patient voice is integrated into corporate affairs, government policy, market access, and communications activities.
Lead the US medical strategy and execution for a specific hematology asset, including launch preparation and evidence generation. Coordinate cross-functional teams to manage clinical studies, advisory boards, and scientific communications.
The Associate Director is accountable for the lifecycle management of drug development and global product development strategies. They drive strategic decision-making, manage program schedules, and coordinate cross-functional teams to deliver goals for patients.
Lead the development and scaling of AI-enabled analytics solutions across Commercial, Medical Affairs, and Clinical Operations to drive data-driven decision-making. Partner with cross-functional leaders to translate complex data into actionable strategies and oversee the responsible adoption of machine learning capabilities.
Lead the strategic design and oversight of GxP compliance and inspection readiness for R&D technology solutions. This includes embedding validation-by-design into Agile workflows and orchestrating live health authority inspections.
Acts as the strategic bridge between R&D and Enterprise IT to align business-specific systems with global infrastructure and security standards. Oversees the engineering of externally developed platforms, AI architectures, and high-performance computing environments to support cancer research.
Lead the ecosystem of externally developed digital and technology platforms for the Global Development function within R&D. Develop and execute the digital technology strategy, managing roadmaps, vendor relationships, and the integration of AI/ML capabilities to accelerate scientific milestones.
Lead the Corporate Affairs and Communications strategy in Germany to strengthen the company's reputation and stakeholder relationships. Represent the organization among government officials, healthcare organizations, and patient groups to improve patient access and outcomes.
Responsible for drafting, negotiating, and finalizing complex clinical site contracts and budgets throughout the study lifecycle. Acts as the primary liaison between clinical operations, legal teams, and investigator sites to ensure timely execution and compliance.
Leads the development and execution of clinical trial supply strategies to ensure continuous drug supply to patients while minimizing waste. Manages relationships with external supply partners and oversees label, pack, and distribution activities within a GxP environment.
The Internal Auditor executes operational, compliance, and SOX audits, including planning, fieldwork, and reporting. The role involves partnering with business owners to manage risks and contributing to advisory projects and audit automation.
Develop and implement statistical analysis plans (SAP) and study protocols for hematology clinical trials. Collaborate with cross-functional teams to analyze data, interpret results, and prepare reports for health authority submissions.
Oversees clinical monitoring activities and manages the CRA team to ensure compliance with ICH-GCP and company SOPs. Leads resource allocation, performance management, and strategic initiatives to optimize clinical operations and trial delivery.
The role focuses on shaping the strategic direction of clinical development in Malaysia and Singapore through feasibility assessments and site engagement. It involves collaborating with cross-functional teams and KOLs to optimize patient enrollment and trial success.
Lead the stewardship of critical Pharma R&D data domains to ensure data quality, compliance, and usability across the research value chain. Manage a team of data stewards to operationalize governance standards and deliver trusted data products for AI/ML and business insights.
The Associate Director will lead strategic drug sourcing initiatives and develop sourcing frameworks to support global clinical trials. This role involves driving innovation in comparator sourcing and optimizing the supplier ecosystem.
The Director will define and execute end-to-end companion diagnostics (CDx) strategies aligned with clinical development programs. This includes partnering with cross-functional teams and external vendors to ensure regulatory approval and successful commercial launch of diagnostic kits.
The CRA performs monitoring activities for Oncology and Hematology clinical trials, including site initiation, routine monitoring, and closeout visits. They ensure data quality and adherence to GCP, ICH, and local regulatory standards while managing site communications and performance.
Lead financial planning, budgeting, and forecasting for Global Enabling Functions while serving as a strategic partner to executive leadership. Drive resource optimization and provide performance insights to support decision-making across global markets.
The Regional Manager is responsible for achieving business goals by partnering with healthcare practitioners to facilitate the appropriate use of Brukinsa. This includes developing regional stakeholder engagement plans and serving as a scientific resource in heme-oncology.
Lead the development of early and late phase clinical strategies for breast cancer assets in collaboration with internal and external partners. Oversee clinical programs, manage regulatory submissions, and lead the growth and mentoring of the Clinical Development team.
Develop and deliver advanced analytics, AI-enabled insights, and predictive models to support data-driven decision-making across Commercial, Medical Affairs, and Clinical Operations. Translate complex longitudinal healthcare data into actionable insights regarding the patient journey, from diagnosis to treatment adherence.
Manage biomarker operational activities for clinical trials, including vendor relationships, bio-sample testing, and budget control. Lead the US biomarker operation team and coordinate cross-functional initiatives to implement biomarker and CDx strategies.
Develop global study strategic feasibility proposals and provide data-driven operational insights to optimize study design and site selection. Partner with cross-functional stakeholders to identify recruitment risks and implement mitigation strategies to accelerate study execution.
This role manages the strategic sourcing and category management of CRO and FSP outsourcing to improve cost efficiency and quality in R&D. It involves leading vendor governance, negotiating MSAs, and partnering with internal stakeholders to optimize external resourcing strategies.
The role focuses on identifying and optimizing digital tools, AI, and systems to enhance Field Medical performance and HCP engagement. It involves collaborating cross-functionally to implement tracking metrics, KPIs, and standardized onboarding processes for field teams.
Manage and coordinate regulatory submissions, including INDs and NDAs, to ensure timely product registration in the US and abroad. Provide regulatory strategy guidance to cross-functional teams and maintain the regulatory archive.
Accountable for the operational performance and optimization of end-to-end distribution and order-to-cash processes in Germany. Acts as the central coordination point for distribution intelligence, ensuring regulatory compliance and alignment across internal and external stakeholders.
Provide strategic and operational leadership for the Regional Clinical Study Management function across Southeast Asia, managing both internal teams and Functional Service Providers. Ensure the successful delivery of the regional clinical trial portfolio in compliance with ICH-GCP and company quality standards.
The Senior Medical Manager leads local medical initiatives and evidence generation to align with global oncology strategies. They provide medical oversight for clinical trials and maintain strategic partnerships with key external stakeholders and KOLs.
Lead the global technology service management strategy, overseeing the ServiceNow platform and global service desk operations to improve reliability and employee productivity. Establish governance frameworks and AI-enabled service delivery models to ensure scalable, high-quality technology services worldwide.
The Director is responsible for executing the Corporate Affairs and Communications strategy for BeOne in the UK and Ireland to establish the company as a valued partner. This includes managing relationships with government officials, healthcare organizations, and patient advocacy groups to enhance company reputation and product awareness.
The Country Medical Director leads the Medical Affairs organization in Germany, overseeing the local medical strategy and ensuring alignment with European and Global priorities. The role involves providing scientific leadership, managing external stakeholder relationships, and ensuring compliance with regional and corporate directives.
Responsible for maximizing product performance in Region North by developing and implementing go-to-market and brand commercial strategies. This includes managing budgets, leading omnichannel tactical plans, and collaborating with cross-functional teams to drive hemato-oncology market growth.
Define and lead the strategy for next-generation customer experience technologies for individuals affected by CLL. Partner with cross-functional teams to deliver scalable, compliant digital products that connect patients and HCPs to clinical trials.
Manage a $50M annual spend portfolio across HR, Translation, and Printing services globally. Lead sourcing initiatives, optimize the supply base, and develop category strategies to align with business priorities.
Provide leadership and line management to regional clinical study teams, ensuring trials are delivered on time and with high quality. Drive the regional Clinical Operations strategy, manage resources, and collaborate with global stakeholders to meet business goals.
Provides strategic leadership and oversight for regional clinical study management, ensuring trials are delivered on time, within budget, and in compliance with quality standards. Manages regional clinical operations teams and acts as the primary point of escalation for portfolio issues.
Provide legal support for the German affiliate and international projects, focusing on contract, pharmaceutical, and labor law. Represent the company in legal disputes and manage external legal counsel while providing internal legal training.
Define and execute the commercial capability-building strategy to support current brands and upcoming product launches in Germany. Lead the design and rollout of new selling models and high-impact training programs for field and cross-functional teams.
Responsible for maintaining the local Quality Management System and ensuring full compliance with Israeli Ministry of Health and global quality standards. This includes performing Qualified Person functions for batch certification and providing quality oversight for importation and distribution activities.
Manage the full-cycle recruitment process for various functional areas across Europe, from developing job descriptions to onboarding. Partner with hiring managers and HRBPs to implement creative sourcing strategies and ensure compliance with government regulations.
The Principal Clinical Datawarehouse Programmer develops and supports ETL data pipelines to ensure high-quality clinical data for business decision-making. This role involves translating user requirements into design specifications and collaborating with cross-functional stakeholders to maintain data governance and security.
Lead the global technology strategy for enabling functions, including HR, Legal, and Corporate Communications, to drive scalability and automation. Oversee the implementation of AI-driven insights and enterprise platforms to optimize corporate operations and data-driven decision-making.
Develop and execute enterprise medical strategies at priority US health systems and oncology networks to address system-level healthcare priorities. Serve as the primary scientific interface for C-suite leadership, coordinating the full oncology portfolio and scientific resources.
Lead and develop the Scientific Partnership Medical Director team while personally managing a portfolio of priority US health systems and oncology networks. Act as the primary architect for enterprise health system engagement strategies to position Medical Affairs as a strategic partner.
Develop and execute enterprise medical strategies at priority US health systems and oncology networks to address system-level healthcare priorities. Serve as the primary scientific interface for C-suite leadership, coordinating the full oncology portfolio across multiple tumor types.
Manage daily technical operations and 'Keep the Lights On' (KTLO) activities for field tools supporting Commercial and Medical Affairs teams. Oversee vendor performance, service quality standards, and the end-to-end technical support process for field applications.
Operationalize AI capabilities across Commercial and Medical teams by defining the semantic layer and implementing RAG-based chat interfaces. Coordinate cross-functional guardrails and build prototypes to turn AI concepts into practical business capabilities.
Lead the strategic definition and execution of site feasibility and engagement across the Americas clinical development portfolio. Focus on optimizing site selection, enrollment planning, and patient recruitment to accelerate trial activation.
Provide strategic statistical solutions and quantitative support for EU HTA submissions and Joint Clinical Assessments. Collaborate with cross-functional teams to build models and ensure organizational readiness for HTA requirements.
Develop and execute Key Opinion Leader (KOL) strategies to support hematology oncology products across the South Central region. Collaborate with cross-functional teams to drive brand objectives and implement commercial strategic plans at scientific meetings.
Drive and manage key cross-functional commercial and medical projects across North America to align with strategic priorities. Lead digital transformation and AI-enabled initiatives to improve productivity and customer engagement within a regulated environment.
The role is responsible for implementing and maintaining a global GVP Quality Assurance framework to ensure pharmacovigilance activities comply with regulatory requirements. Key duties include leading PV inspection readiness, managing quality systems, and overseeing vendor audits.
Serve as a strategic analytics partner to support the launch and growth of BEQALZI and BTK CDAC by generating actionable insights. Lead analytics across commercial performance, customer segmentation, and market dynamics to inform critical business decisions.
Manage local pharmaceutical affairs, including regulatory and quality assurance operations, acting as a contact for competent authorities in Germany. Oversee GxP governance, product labeling, distribution activities, and the review of promotional materials.
Lead the end-to-end management of escalated GxP and Quality incidents globally, ensuring root cause identification and the implementation of CAPAs. Develop and maintain quality risk management frameworks and knowledge management tools to ensure regulatory compliance and patient safety.
The Director will lead Medical Governance and Operations, focusing on the standardization of operational activities and project management support for the Global Medical Affairs Leadership Team. They are accountable for Medical Review, Education Grants, and Contracting processes across Global and US markets.
Scale the Enterprise Information Architecture framework and translate strategic vision into scalable data products for R&D and enterprise decision-making. Lead initiatives in Master Data Management, data quality, and semantic modeling across Clinical Operations, Safety, and Regulatory domains.
Responsible for developing high-quality clinical and regulatory documents to support the development and approval of products in the oncology pipeline. This role involves leading document strategy, managing timelines for complex submissions, and mentoring junior medical writers.
Lead the design and scaling of enterprise AI platforms, focusing on RAG, agentic AI frameworks, and LLM-powered services. Partner with cross-functional teams to transition AI experiments into production-ready capabilities for Commercial and Medical Affairs.
The Regional Manager will develop and execute regional plans, promote BeOne’s products, and provide education to healthcare professionals. They will also ensure compliance with laws and regulations while managing administrative functions.
Lead and mentor a regional team of clinical study managers to ensure the timely and high-quality delivery of clinical trials. Drive the regional clinical operations strategy, manage resourcing, and collaborate with global stakeholders to meet business goals.
Oversees internal operations for Clinical Operations Americas, providing leadership in finance, resource management, and metrics development. Acts as the primary support to the Americas Clinical Operations Head to drive operational excellence and productivity.
The SCRA is responsible for managing and overseeing clinical study sites to ensure data quality and patient safety in accordance with ICH-GCP guidelines. They also provide mentoring to junior CRAs and collaborate with Clinical Study Teams to optimize site effectiveness and efficiency.
The Director of Field Tools serves as a strategic partner for Commercial and Medical Affairs to manage the implementation and optimization of Field BI tools and technology platforms. They are responsible for driving tool adoption, streamlining business processes, and overseeing technical operations to support oncology portfolio commercialization.
Oversees clinical monitoring activities and manages the CRA team to ensure compliance with ICH-GCP and company SOPs. Leads resource allocation, performance management, and strategic initiatives to optimize clinical operations and trial delivery.
Coordinate and manage language and translation projects from initiation to delivery. Liaise with internal stakeholders and external global vendors to ensure content is linguistically correct and faithful to the original intent.
Serve as the primary Compliance and Risk Management lead for Germany, ensuring adherence to local codes, regulations, and company policies. Provide strategic guidance to internal teams on interactions with healthcare professionals and oversee ABAC controls and internal monitoring plans.
The intern will support Regulatory Affairs CMC projects by maintaining accurate information in the RIM system and assisting with data remediation. They will also contribute to the drafting of CTD CMC sections for global health authority submissions.
The Executive Director will develop and implement global medical strategies for hematology assets, focusing on CLL, lymphomas, and Waldenstrom Macroglobulinemia. They will lead cross-functional teams, oversee evidence generation, and manage external collaborations to support product launches and lifecycle management.
The Associate Director, Safety Scientist leads the identification, analysis, and evaluation of safety signals to manage risk profiles for developmental and marketed products. They also provide safety expertise for clinical trials, regulatory submissions, and the maintenance of safety documentation in compliance with global standards.
The Director will lead cross-functional collaborations to drive cost optimization, innovation, and strategic budget planning for R&D pipelines and partnerships. They will provide data-driven insights through advanced analytics and benchmarking to enhance operational capacity and competitive positioning.
The Senior Medical Director will contribute to clinical development strategy and oversee medical monitoring for pivotal stage oncology studies. They will collaborate with cross-functional teams to ensure successful execution of clinical programs within scope, budget, and timelines.
The role leads the global forecasting and commercial performance management Center of Excellence to drive high-quality decision-making and strategic planning. This leader establishes governance, standards, and best practices while managing a high-performing team to ensure forecast accuracy and transparency across the organization.
Lead and mentor the oncology program management team to drive global clinical development strategies and project execution. Facilitate cross-functional alignment, manage project budgets, and implement process improvements to optimize team efficiency and quality.
The role involves designing, planning, and leading statistical analyses for Real-World Data (RWD) and Real-World Evidence (RWE) studies, including comparative effectiveness and safety assessments. Responsibilities also include overseeing and validating statistical programming deliverables, performing analyses in big data environments, and applying AI capabilities to enhance workflows.
The Associate Director will serve as the clinical biomarker lead for assigned immunology programs, responsible for designing and executing mechanism-driven clinical biomarker strategies to inform patient selection and key clinical decisions. This role involves providing translational and biomarker leadership across clinical development, contributing as a core team member to advance early- and late-stage programs.
This senior director will lead and continuously strengthen the U.S. Biologics Regulatory CMC team, providing strategic and operational leadership for global CMC regulatory strategies across the product lifecycle, including oversight of CTD sections for major submissions.
The Business Operations Director is responsible for driving operational excellence and coordinating projects to optimize BeOne’s in-market portfolio performance. This includes overseeing operational planning, managing resources, and ensuring effective execution of initiatives.
The Associate Director will lead the strategic growth and operational excellence of SAP Finance capabilities for BeOne’s EMEA operations. This includes defining the global vision for SAP Finance solutions and ensuring compliance with local statutory requirements.
The Director, Global Regulatory Lead develops, implements, and advises on global regulatory strategies to secure and maintain market access for products in alignment with business objectives. This role manages regulatory aspects through all development phases, post-approval, and life-cycle, providing strategic oversight and acting as an advisor/liaison to global project teams.
