The Senior Study Start-Up Manager is responsible for the delivery of clinical trial start-up activities, including site identification, feasibility, and activation within established timelines and quality standards. The role also involves line management of staff, process improvement initiatives, and ensuring compliance with ICH/GCP and local regulations.
The Senior Study Start-Up Manager is responsible for the delivery of clinical trial start-up activities, ensuring quality and adherence to ICH/GCP and local regulations. They also provide line and functional management to team members while driving process improvements across the Americas region.
The Manager, CDx Development, oversees CDx portfolio and project management within the Precision Medicine Team while supporting diagnostics alliance management. Key duties include coordinating project timelines, managing budgets, tracking risks, and maintaining documentation to ensure effective collaboration with internal and external partners.
The Senior Regional Clinical Compliance Manager ensures robust oversight of clinical trial compliance at the country and site level using a risk-based approach. They serve as a subject matter expert, managing compliance risks, supporting audits, and facilitating corrective and preventive actions.
The Associate Director will lead the development and modernization of enterprise R&D resource and costing tools for clinical trials. They will act as a product owner to integrate these tools with internal systems like CTMS, SAP, and Workday to ensure accurate financial forecasting and operational efficiency.
The Associate Director will lead global clinical biomarker strategies for solid tumor oncology programs, overseeing assay development and data interpretation. They will also manage external partnerships and contribute to regulatory submissions to support pipeline advancement.
The Associate Director will collaborate with cross-functional teams to develop statistical analysis plans and support the design and interpretation of clinical trials. They will also ensure data quality, coordinate statistical activities, and communicate results to regulatory agencies and project teams.
The Manager, R&D Data Steward leads stewardship activities for assigned R&D data domains, ensuring data is well-defined, discoverable, and governed. This role involves collaborating with stakeholders to implement data standards, perform data profiling, and leverage AI-assisted tools to improve data quality and usability.
The Marketing Director is responsible for building and leading the marketing function to develop and execute commercialization strategies for Haematology products in the UK and Ireland. This role involves collaborating with cross-functional teams, managing budgets, and coaching the marketing team to drive high performance.
The Associate Clinical Research Manager oversees clinical monitoring activities and the CRA team to ensure compliance with ICH-GCP and company SOPs. This role is responsible for resource allocation, performance management, and fostering team development to achieve organizational goals.
The Associate Director will enhance Global Clinical Operations productivity by optimizing digital solutions like the Clinical Trial Management System (CTMS). They will facilitate stakeholder engagement, manage project requirements, and drive the implementation of innovative technology roadmaps.
The Regional Clinical Study Manager is responsible for the regional delivery of clinical studies, ensuring they meet quality, timeline, and budget requirements. They lead regional clinical operations teams, manage external vendors, and ensure inspection readiness across all study sites.
The Executive Director will lead the Global Medical Affairs Companion Diagnostic (CDx) strategy to support clinical and medical assets. They will collaborate cross-functionally to integrate CDx programs, manage data generation, and engage key opinion leaders to ensure successful launch readiness.
The Field Medical Director will develop regional strategies to support pipeline development for solid tumor assets while establishing credible peer-to-peer relationships with healthcare providers and opinion leaders. They will also facilitate strategic partnerships, support clinical trials, and provide scientific information to internal and external stakeholders.
The Global Commercial Lead will drive launch preparations and readiness for the GI franchise, mobilizing the Global Brand Team to execute global commercial strategies. This role serves as the primary commercial voice within the Global Product Team, ensuring alignment across R&D, regional partners, and executive leadership.
The Associate Director will support the development and operationalization of the COHERE strategy to improve patient access to clinical research across the trial lifecycle. They will partner cross-functionally to integrate patient access considerations into study planning, site selection, and enrollment performance monitoring.
The Associate Director is responsible for establishing and maintaining the Local Quality Management System for the Turkish affiliate to ensure full regulatory compliance. They will act as the Qualified Person, overseeing GMP/GDP operations, third-party logistics providers, and managing quality governance for the Turkish market.
The Country Medical Director leads medical strategy and team management in Austria, supporting product development, launch, and lifecycle management. They act as the primary scientific liaison with healthcare experts and ensure alignment between local, regional, and global medical objectives.
The Country Manager is responsible for defining and executing the strategic business plan for the Nordics region to achieve revenue and growth targets. They lead a diverse management team, manage stakeholder relationships, and ensure compliance across all GxP areas while driving patient-focused commercial success.
The Director leads the global PV Alliance and Contract Management team to ensure strategic alignment and compliance across pharmacovigilance partnerships. This role oversees the negotiation, implementation, and lifecycle management of PV contracts while serving as a key advisor to internal and external stakeholders.
The Regional Clinical Compliance Manager ensures robust oversight of clinical trial compliance at the country and site level by applying a risk-based approach. They serve as a subject matter expert, manage compliance issues, and support audit and inspection readiness.
The role focuses on leading executive talent scouting initiatives for specialized scientific positions and developing strategic talent pipelines. It also involves conducting market intelligence, building scientific networks, and managing long-term relationships with research leaders.
The Senior Director will serve as the lead compliance business partner for the U.S. Commercial organization, focusing on Market Access and strategic risk management. They will provide guidance on complex healthcare compliance matters, lead risk assessments, and develop policies to support responsible innovation.
The Senior Manager is responsible for developing and executing HCP and DTC promotional assets to support the growth of the BRUKINSA brand. They will manage cross-functional relationships and oversee the promotional review process to ensure all materials meet regulatory and business objectives.
The Program Lead oversees clinical data management activities for multiple studies and programs, ensuring data quality, compliance, and adherence to timelines. They collaborate with cross-functional teams and vendors while driving process improvements and standardization initiatives.
The Senior Manager leads clinical studies and programs from a data management perspective, ensuring data quality, compliance, and operational efficiency. They collaborate with cross-functional teams and vendors to manage timelines, develop study documentation, and drive process improvement initiatives.
The Clinical Research Associate is responsible for executing clinical monitoring activities at trial sites in accordance with ICH-GCP guidelines and local regulations. They manage site performance, ensure data quality, and collaborate with the Regional Clinical Operations Manager to meet study milestones.
The Senior Manager, Biostatistics develops statistical methodologies for RWD/RWE studies and analyzes large datasets from diverse sources. They also collaborate with cross-functional teams to ensure high-quality data collection and provide statistical consultation for clinical and commercial projects.
The Key Account Manager is responsible for maximizing product presence in the heme-oncology market by implementing marketing strategies and achieving sales targets. They will develop strategic account plans, build relationships with key stakeholders, and organize local symposia to optimize patient care.
The Senior Medical Science Liaison acts as a field-based medical representative to build relationships with healthcare professionals and key opinion leaders. They are responsible for exchanging scientific information, collecting medical insights, and supporting clinical trial activities within their assigned territory.
The Senior Clinical Research Associate manages and oversees clinical trials to ensure high-quality data collection in compliance with GCP and regulatory standards. They are responsible for monitoring site performance, verifying data integrity, and collaborating with study teams to meet project milestones.
The Manager, Safety Scientist supports signal detection, safety data evaluation, and the preparation of regulatory-required periodic reports for assigned compounds. They collaborate with cross-functional teams to ensure safety monitoring throughout clinical trials and contribute to global regulatory submissions.
The Global Clinical Study Senior Manager is accountable for the end-to-end operational delivery of clinical studies, ensuring execution excellence across all regions. This role leads global clinical operations teams, manages study strategy, and maintains oversight of timelines, quality, and budgets.
The Regional Clinical Compliance Manager is responsible for implementing global compliance and inspection management strategies across clinical activities. They provide oversight, conduct site compliance visits, and ensure adherence to regulatory requirements and internal SOPs.
The Senior Medical Science Liaison is responsible for delivering high-quality scientific exchange with healthcare professionals and managing relationships with Key Opinion Leaders. They also support clinical trial activities, provide medical insights to internal stakeholders, and collaborate cross-functionally to execute medical plans.
The Clinical Research Associate executes clinical monitoring activities at trial sites in accordance with ICH-GCP guidelines and local regulations. They are responsible for managing site performance, ensuring data quality, and collaborating with the Regional Clinical Operations Manager to meet study milestones.
The Corporate Account Director is responsible for developing and implementing strategic business plans to expand relationships with key oncology stakeholders in the Northeast region. They will collaborate with cross-functional teams to remove barriers to product access and ensure successful contract pull-through for solid tumor products.
The Regional Clinical Compliance Manager ensures robust oversight of clinical trial compliance at the country and site level using a risk-based approach. They serve as a subject matter expert, managing compliance issues, supporting audits, and ensuring adherence to GCP and regulatory standards.
The Senior Director will lead clinical development programs for solid tumors, overseeing strategy, execution, and cross-functional collaboration. They are responsible for authoring key clinical documents, managing study budgets, and building relationships with external investigators and partners.
The Executive Director will lead global commercial strategies for Tacabrutideg, ensuring alignment across cross-functional teams and regional markets. They are responsible for driving long-term product success, managing brand lifecycle strategies, and representing the commercial voice to executive leadership.
The Senior Manager leads global regulatory compliance programs, including inspection readiness, risk management, and regulatory information quality. They partner with cross-functional teams to ensure processes and systems remain compliant with global health authority expectations.
The Associate Director of Digital Execution will lead the development and execution of digital and non-personal promotion strategies for the BRUKINSA brand. This role involves managing cross-functional collaborations, overseeing agency relationships, and monitoring campaign performance to drive brand growth.
The Clinical Research Manager oversees clinical monitoring activities and the CRA team to ensure compliance with ICH-GCP and regulatory standards. This role is responsible for team resource allocation, performance management, and fostering site relationships to achieve study deliverables.
The role involves developing and executing market access strategies to ensure sustainable access to the oncology and haematology portfolio in Australia and New Zealand. You will lead PBAC submissions and provide technical pricing support while collaborating with cross-functional teams to inform business planning and launch readiness.
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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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.
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 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.
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.
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 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.
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 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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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 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 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.
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.
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.
