The Clinical Research Associate II conducts site visits to ensure protocol compliance, data quality, and patient safety in accordance with ICH-GCP guidelines. They also manage site relationships, provide training, and oversee site performance metrics to ensure timely delivery of study milestones.
Develop and improve AI-enabled decision products and analytical solutions for Clinical Development and Operations, using trusted data, advanced analytics, and business context. Collaborate with cross-functional teams to evaluate AI quality, track product adoption and business outcomes, and translate findings into actionable recommendations.
The CRA will conduct site visits, manage site relationships, and ensure protocol compliance and data quality in accordance with ICH-GCP guidelines. They are also responsible for training site personnel, monitoring patient safety, and collaborating with the Clinical Study Team to meet study milestones.
The Senior 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, ensuring data quality, and collaborating with clinical study teams to meet study milestones.
The Marketing Lead is responsible for defining the portfolio and brand strategy for Solid Tumors in Germany, including leading launch plans and cross-functional execution. They will also manage brand budgets, oversee agency relationships, and lead a small team to drive commercial performance.
The QC Specialist coordinates and completes quality reviews of clinical and regulatory documents to ensure scientific accuracy and compliance with standards. They perform data verification, proofreading, and cross-referencing while maintaining strict project timelines.
Conduct clinical trial monitoring at assigned oncology and hematology sites, from feasibility and study start-up through recruitment, routine monitoring, and closeout, in compliance with ICH-GCP, local regulations, and company procedures. Track site performance and study milestones, maintain inspection readiness, communicate progress and issues, and identify quality gaps and corrective actions in collaboration with clinical operations teams.
The Sr. Principal Software and AI Engineer will architect and deploy AI-powered agentic applications to accelerate clinical trial execution and protocol generation. This role involves setting technical standards for AI-native development, ensuring GxP compliance, and providing leadership to cross-functional engineering teams.
Promote oncology and hematology products to healthcare professionals while managing relationships with key accounts, including wholesalers and payers. Analyze market needs, collaborate with commercial and medical teams on sales strategies, maintain CRM records, and independently manage field schedules and travel.
Lead the strategy, requirements, deployment, adoption, and continuous improvement of digital platforms and workflows supporting US Field Medical, including AI-enabled Next Best Action capabilities and CRM systems. Partner across Medical, IT, content, and technology teams to improve HCP engagement planning, reporting, insights, impact measurement, compliance, and user adoption.
The Associate Director will lead the UK Regulatory Affairs team to develop and implement regulatory strategies for development programs and commercial products. They are responsible for managing regulatory agency communications, preparing MAA dossiers, and ensuring compliance with UK and Ireland regulatory requirements.
Lead the global product strategy for a lung cancer asset across its entire lifecycle, from early clinical development through commercial launch and post-marketing. Build and manage a high-performing cross-functional team to drive program vision, secure governance funding, and maximize the asset's value.
The Senior Global Clinical Study Manager is responsible for leading global cross-functional study teams to deliver clinical trials within agreed timelines, budget, and quality standards. They oversee external vendors, manage study documentation, ensure inspection readiness, and act as the primary point of escalation for study-related issues.
Lead the strategy, commercial performance, and P&L of the country’s solid tumor franchise, overseeing sales and marketing from launch planning through commercialization and lifecycle management. Build market-driven plans, manage budgets and teams, and collaborate with local, regional, and global partners to grow the business while meeting compliance standards.
The CRA is responsible for monitoring clinical trial activities, including site initiation, recruitment, and data quality, to ensure adherence to GCP and regulatory standards. They also manage site performance, facilitate contract negotiations, and provide protocol training to ensure study milestones are met.
The Case Manager supports the patient support program by educating stakeholders and managing the specialty pharmacy distribution network to ensure patient access to therapy. They also triage reimbursement issues and collaborate with internal teams to resolve barriers and maintain patient compliance.
The Senior Director leads the global strategy, governance, and operational execution of clinical site contracting to ensure efficient study startup and compliance. They manage a global team, oversee contract lifecycles, and collaborate with cross-functional stakeholders to drive process improvements and financial performance.
The Senior Manager will lead R&D financial planning, monthly close, and consolidation processes while providing strategic decision analysis for pipeline investments. They will partner cross-functionally to deliver financial insights and enhance reporting efficiency through automation and modern financial tools.
The Senior Contracts Associate is responsible for drafting, negotiating, and finalizing complex clinical site contracts and amendments throughout the study lifecycle. They also manage budget grids, ensure compliance with legal and regulatory requirements, and serve as the primary point of contact between internal operations and external sites.
The Associate Director will partner with leadership to scale enterprise information architecture, defining data domains and canonical models to support R&D and enterprise decision-making. They will drive the execution of strategic data initiatives, ensuring the delivery of trusted, governed, and scalable data products across clinical and regulatory domains.
The Associate Director will build and scale enterprise data governance capabilities by operationalizing stewardship within a federated model. They will partner with cross-functional teams to ensure data assets are trusted, compliant, and aligned with business and AI readiness objectives.
The Senior Manager will own the enterprise Master Data Management (MDM) program and drive innovation in data governance and reference data management. They will lead development teams, manage stakeholder requirements, and develop metrics to demonstrate the impact of data activities.
The Associate Director is responsible for developing and executing Key Opinion Leader (KOL) strategies to support the hematology oncology portfolio within the South Central region. They will collaborate with cross-functional teams to drive commercialization, manage promotional programming, and provide market insights to ensure brand success.
The Senior Administrative Assistant provides proactive administrative support to assigned functions, including complex calendar management, travel arrangements, and meeting coordination. The role also manages vendor onboarding, expense reporting, and assists with the onboarding process for new employees.
The associate supports the Regional Clinical Study Manager in the execution and delivery of clinical studies within specified quality, timeline, and budget standards. Responsibilities include managing study start-up activities, maintaining clinical systems, and collaborating with cross-functional teams to ensure operational excellence.
The Director is responsible for leading GCP inspection readiness, hosting regulatory inspections, and developing proactive risk-based inspection strategies. They will manage a team of quality professionals and collaborate cross-functionally to ensure compliance and continuous improvement across R&D quality systems.
The Associate Director drives global value, access, pricing, and reimbursement launch-readiness for hematology assets across geographies. They collaborate with cross-functional teams to develop access toolkits and translate evidence into differentiated pricing strategies.
The Senior Manager is responsible for the day-to-day operational health, lifecycle execution, and compliant management of Veeva platforms within the global R&D technology portfolio. They coordinate matrixed technical resources and vendors to ensure systems remain secure, reliable, and aligned with business needs.
The Associate Director drives global value, access, pricing, and reimbursement strategies for hematology assets to ensure timely launch readiness and optimal patient access. They collaborate with cross-functional teams to develop country-ready toolkits and translate payer insights into actionable clinical and commercial strategies.
The Regional Contracts Lead is responsible for the oversight and execution of clinical contract agreements, including CTAs and site budgets, across the region. They provide functional line management to the contracts team and serve as a regional escalation point to ensure compliance and operational efficiency.
The Director will lead the development and scaling of advanced analytics and AI-enabled solutions to support decision-making across Commercial, Medical Affairs, and Clinical Operations. This role involves partnering with cross-functional teams to translate complex data into actionable insights while championing responsible AI practices and data governance.
The Director is responsible for executing the global medical plan for sonrotoclax, ensuring all activities are patient-centered and evidence-driven. This role involves managing scientific exchange, evidence generation, and cross-functional collaboration across global and regional teams.
The Director is responsible for executing the global medical plan for zanubrutinib, ensuring all activities are patient-centered and evidence-driven. This role involves managing medical activities throughout the product lifecycle, supporting scientific exchange, and collaborating with cross-functional teams.
The Senior Director leads the global ERP Center of Excellence delivery function, defining governance, standards, and execution strategies for SAP-related projects. They are responsible for managing capacity, quality, release cycles, and continuous improvement across a globally distributed team.
The role provides coordination and operational support to Process Leads and senior GCPM leadership to ensure effective execution of process management activities and document control workflows. The incumbent also analyzes data from source systems to facilitate decision-making, process progression, and continuous improvement initiatives.
The manager will execute strategies for monitoring and submitting individual case safety reports and aggregate safety reports to regulatory authorities and partners. They will also analyze compliance metrics and collaborate with cross-functional teams to ensure adherence to global safety reporting obligations.
The Senior Director leads global Patient Reported Outcomes (PRO) strategy to demonstrate the humanistic value of therapies across the product lifecycle. They oversee integrated evidence generation, provide scientific leadership, and influence cross-functional teams to ensure PRO perspectives are embedded in clinical and commercial strategies.
The Global Clinical Process Management Lead is responsible for overseeing global clinical process management activities to ensure efficiency, consistency, and regulatory compliance within Global Clinical Operations. This role involves leading process initiatives, managing document workflows, and collaborating with cross-functional stakeholders to implement continuous improvements.
The specialist is responsible for the end-to-end delivery of study start-up activities, including site selection, activation, and regulatory submissions. They ensure high-quality document management and compliance with ICH/GCP guidelines and internal SOPs.
The Regional Clinical Study Manager is accountable for regional study delivery, ensuring inspection readiness, quality, 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 within the region.
The Associate Director is responsible for the regional delivery of clinical studies, ensuring quality, budget adherence, and inspection readiness. They lead regional clinical operations teams, manage vendor relationships, and drive study execution from feasibility through closeout.
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 Senior Director of Regulatory Affairs is responsible for developing and executing U.S. regulatory strategies and leading FDA interactions across the development portfolio. They provide strategic leadership, manage regulatory risks, and ensure cross-functional alignment to achieve timely product approvals and lifecycle success.
The Product Quality Lead will drive global quality initiatives, manage quality risk assessments, and oversee cross-functional collaboration for late-phase clinical and commercial programs. This role also involves serving as a Subject Matter Expert for regulatory submissions, quality investigations, and the implementation of robust quality governance frameworks.
The Head of Patient Recruitment and Retention is responsible for designing and executing comprehensive strategies to enroll and retain patients in clinical trials across the Americas. This role involves managing vendor partnerships, collaborating with patient advocacy groups, and utilizing data-driven insights to optimize trial performance.
The Senior Medical Writer is responsible for writing, editing, and formatting clinical regulatory documents to ensure they meet domestic and international standards. They must collaborate with cross-functional teams to maintain project timelines and ensure the scientific accuracy of all regulatory submissions.
The Regional Clinical Study Manager is responsible for the regional delivery of clinical studies, ensuring quality, adherence to timelines, and budget management. They lead the regional clinical operations team, oversee external vendors, and ensure compliance with regulatory standards and study protocols.
The Associate Director provides leadership and management to clinical study managers while contributing to regional clinical operations strategy and performance metrics. They are responsible for ensuring quality, managing budgets, and overseeing resourcing to ensure clinical trials are delivered on time and in alignment with organizational goals.
The Senior Manager will lead the planning, coordination, and preparation of regulatory submissions, including INDs and BLAs/NDAs. They will also represent Regulatory Affairs on cross-functional project teams to provide strategic guidance and ensure compliance with global regulatory requirements.
The Associate Director will lead early patient engagement and evidence generation strategies to integrate patient perspectives into medical strategy and clinical development. They will manage cross-functional partnerships and external relationships with professional societies to ensure patient-centered drug development.
Deliver systems engineering work across R&D platforms, cloud and hybrid infrastructure, integrations, high-performance computing, and foundational AI architectures, ensuring solutions meet enterprise security, compliance, and operational standards. Coordinate with Enterprise IT, vendors, and R&D stakeholders; maintain technical plans and documentation, support operational readiness, and escalate risks and dependencies.
Develop and execute strategic and tactical sales plans to exceed goals, while overseeing division strategy, resource allocation, hiring, and performance management. Recruit and lead Hematology Sales Representatives, build a culture of continuous learning, and collaborate across commercial teams to strengthen customer relationships and team results.
Build and maintain scientific partnerships with healthcare professionals, key opinion leaders, clinical sites, and other stakeholders across East Germany, providing accurate, non-promotional medical information on BeOne’s oncology products and pipeline. Gather and communicate medical insights, support clinical research and evidence generation, and collaborate with Medical Affairs and cross-functional teams to plan and deliver regional medical strategies and activities.
The specialist is responsible for managing study start-up activities in Germany and Austria, including regulatory submissions and site documentation. They collaborate with clinical study managers to ensure timelines are met and maintain high quality and integrity standards across study sites.
The Senior Director will lead global HEOR and RWE strategy for BRUKINSA to support value demonstration, reimbursement, and market access across hematology indications. They will collaborate cross-functionally to design evidence generation plans, manage research partners, and drive scientific dissemination of data.
The Director will lead global commercial initiatives, including HCP and non-personal promotions, to ensure successful launch readiness for the tacabrutideg brand. They will also develop KOL strategies and collaborate with cross-functional teams to drive global launch excellence.
Coordinate and manage clinical study start-up across multiple sites, including regulatory submissions, informed consent forms, essential documents, budgets, contracts, and protocol amendments. Ensure regulatory compliance, quality, and inspection readiness while addressing site issues and supporting study milestones.
Manage and develop clinical research associates and study start-up staff, including hiring, onboarding, training, performance reviews, workload oversight, and accompanied site visits. Support country-level study start-up and trial delivery by coordinating regulatory submissions, site activation and enrollment, quality and inspection readiness, and resolution of site risks.
The Senior IP Counsel will build and maintain a robust intellectual property portfolio to support the company's R&D, manufacturing, and commercialization efforts for biologics. They will also serve as a strategic partner to senior leadership, providing legal guidance on patent strategy, regulatory data protection, and business development collaborations.
Own and refine the quantitative analytics foundation for R&D portfolio prioritization, valuation, and governance, integrating probability of success, timelines, scenarios, competitive intelligence, and market assumptions. Translate analyses into decision-ready committee materials and narratives, support portfolio review sessions, and partner across strategy, finance, systems, commercial, and data science teams to develop reusable and AI-enabled decision tools.
Execute validation, compliance, and inspection-readiness activities for R&D technology systems, including lifecycle documentation, risk-based testing, vendor assessments, and audit support. Coordinate remediation and readiness tracking while translating regulatory expectations into practical actions for engineering, product, Quality, Compliance, IT, Security, and vendor teams.
The Senior Manager will define and implement market access strategies to optimize the availability of products at regional and hospital levels. They will build strategic relationships with regional payers, health authorities, and medical societies to ensure successful drug positioning and policy influence.
The Director, Process Optimization Lead is responsible for driving operational excellence and continuous process improvement within the Program and Study Management function. This role involves strategic planning, managing cross-functional initiatives, and ensuring clinical study execution aligns with regulatory requirements and business goals.
The Associate Director will focus on secondary data analytics to inform business strategy, field optimization, and commercialization efforts. Key tasks include developing sales force targeting and call plans, managing territory alignments, and providing actionable insights to support senior management.
The Director will own the enterprise legal entity forecasting and reporting framework, ensuring accurate translation of management forecasts into statutory and tax-compliant projections. This role involves partnering with Global Tax, Treasury, and Accounting teams to provide actionable insights and governance across the organization.
The Senior Director is responsible for the global strategy, roadmap, and engineering of the Microsoft 365 environment, ensuring it is secure, reliable, and aligned with enterprise goals. They will lead a global team to manage platform modernization, AI-enabled productivity, and cross-functional governance.
The Senior Director oversees global strategic feasibility and study start-up processes to ensure high-quality clinical study planning and execution. They lead cross-functional teams to optimize study timelines, manage documentation, and drive data-informed decision-making across the organization.
The Senior Field Market Access Manager is responsible for optimizing regional access to the company's therapeutic portfolio by building institutional relationships with payers and healthcare stakeholders. This role involves leading negotiations for tenders and framework agreements while demonstrating the clinical and economic value of products within the regional healthcare environment.
The Medical Science Liaison serves as a field-based scientific expert responsible for building peer-to-peer relationships with healthcare professionals and key opinion leaders. They provide scientific support, gather medical insights, and facilitate evidence generation to advance patient care and support organizational objectives.
The Project Data Manager oversees the clinical trial data management process from study start-up through database lock, ensuring high-quality deliverables and adherence to timelines. This role involves leading clinical studies, managing CRO/FSP vendors, and collaborating with cross-functional teams to maintain data integrity and regulatory compliance.
The Senior Clinical Data Manager oversees all clinical trial data management activities from study startup through database lock. They are responsible for data cleaning, reconciliation, query management, and ensuring the quality of deliverables while supporting study teams.
The Senior Director leads hematology portfolio governance and strategy, facilitating decision-making across R&D, commercial, and finance teams. They manage the Hematology Development Review Committee process and drive annual portfolio prioritization to ensure strategic alignment and operational efficiency.
The Senior Director will lead the enterprise Organizational Change Management strategy to support global technology transformations and organizational readiness. They will advise executive leadership, manage a global OCM team, and ensure alignment across diverse stakeholders to drive adoption and measurable value.
The Key Account Manager is responsible for implementing marketing strategies and achieving sales targets within the Berlin, Brandenburg, and Mecklenburg-Vorpommern regions. They will provide scientific expertise to hospital pharmacists and oncologists while managing commercial projects to optimize patient care.
The Associate Director will lead the Ex-China Commercial Master Data Management capability, overseeing data governance, quality standards, and stewardship programs. This role acts as a business owner for commercial data domains and partners with cross-functional teams to ensure scalable, data-driven decision-making.
The Manager, Safety Scientist supports signal detection, safety data evaluation, and risk management for assigned compounds in compliance with global regulations. They also provide safety expertise for clinical trial documentation and contribute to regulatory submissions and periodic safety reports.
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 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 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 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 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 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, 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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.
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, 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 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.
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.
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.
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.
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.
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 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.
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.
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.
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.
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.
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.
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 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.
