The Executive Director will serve as the Global Brand Leader for two late-stage Lung Cancer assets, overseeing global commercial strategies and launch readiness. They will lead cross-functional Global Brand Teams to drive organizational alignment, develop brand plans, and maximize portfolio value.
BeiGene
156 Remote Job Openings at BeiGene
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.
Associate Director, Patient Services and Distribution Case Management
BeiGene
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Full Time
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3 days ago
BeiGene
The Case Manager supports the patient support program and specialty pharmacy network by managing patient access to therapy and resolving reimbursement issues. They also collaborate with internal stakeholders and healthcare providers to educate them on program offerings and ensure ongoing therapy compliance.
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.
Senior Medical Science Liaison, Solid Tumors - South Germany
BeiGene
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Full Time
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3 days ago
BeiGene
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.
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.
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 Senior Global Clinical Study Manager is responsible for the end-to-end delivery of global clinical studies within budget and timeline constraints while ensuring high-quality inspection readiness. They lead cross-functional study teams, manage external vendors, and oversee all operational aspects from feasibility through study closeout.
Senior Manager, Clinical Site Payments, Portfolio Management
BeiGene
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Full Time
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4 days ago
BeiGene
The Senior Manager oversees global financial management, reconciliation, and portfolio-level governance for investigator grant payments in clinical trials. They are responsible for ensuring accrual integrity, managing financial forecasts, and maintaining compliance with SOX and internal control frameworks.
The Submission Strategy Lead manages regional submission governance, strategy, and risk management for multi-country clinical studies across the EMEA region. They act as the primary interface between regional and country teams to ensure regulatory compliance and efficient study start-up.
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 clinical operations, legal, and external sites to ensure compliance and timely execution of agreements.
The associate supports the Regional Clinical Study Manager in the execution of clinical trials, ensuring quality standards, timelines, and budget adherence. Responsibilities include managing study documentation, coordinating site logistics, and facilitating collaboration across regional and global teams.
The Clinical Supply Chain Specialist manages drug supply activities, including planning, label development, and distribution for clinical trials. They collaborate with internal and external stakeholders to ensure continuous supply to patients while minimizing waste and identifying risks.
The Key Account Manager is responsible for promoting oncology and hematology products to healthcare professionals and driving commercial negotiations within their assigned territory. They must develop and execute local engagement plans, manage customer relationships, and ensure commercial proposals align with patient access needs.
Field Medical Director, Solid Tumor- Breast and Lung Boston/New England
BeiGene
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Full Time
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5 days ago
BeiGene
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 CRA executes clinical monitoring activities at trial sites to ensure compliance with ICH guidelines, GCP, and local regulations. Responsibilities include site selection, initiation, routine monitoring, and mentoring junior staff to maintain study quality and timelines.
The CRA executes clinical monitoring activities at trial sites to ensure compliance with ICH guidelines, GCP, and local regulations. Responsibilities include site selection, initiation, routine monitoring, and mentoring junior staff while collaborating with regional study teams.
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.
Senior Medical Director, Asset Lead, US Medical Affairs-Hematology
BeiGene
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Full Time
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12 days ago
BeiGene
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.
Associate Director, Program Management Office, Global Medical Affairs (ex-China)
BeiGene
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Full Time
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12 days ago
BeiGene
Lead the planning and execution of global medical initiatives and evidence plans for the hematology franchise. Drive operational efficiency within the PMO by implementing standardized processes and performance metrics across Global Medical Affairs.
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.
Director, Advanced Analytics and Data Science - Innovation
BeiGene
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Full Time
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12 days ago
BeiGene
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.
Senior Director, Global Digital & Technology Systems Engineering
BeiGene
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Full Time
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12 days ago
BeiGene
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.
Senior Director, Global R&D Audits & Inspections Readiness
BeiGene
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Full Time
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12 days ago
BeiGene
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.
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.
Responsible for ensuring clinical trial compliance at the country and site level using a risk-based approach. The role involves managing compliance risks, overseeing site health checks, and supporting audit and inspection readiness.
The role is responsible for ensuring clinical trial compliance at the country and site level using a risk-based approach. Key duties include serving as a GCP subject matter expert, managing CAPAs, and supporting audit and inspection readiness.
The role is responsible for ensuring clinical trial compliance at the country and site level using a risk-based approach. It involves serving as a GCP subject matter expert and managing CAPAs to safeguard patient safety and data integrity.
Responsible for ensuring clinical trial compliance at the country and site level using a risk-based approach. The role involves managing compliance risks, overseeing GCP adherence, and supporting audit and inspection readiness.
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.
Develop and implement global regulatory strategies to secure market access for oncology products throughout their development and lifecycle. Provide strategic oversight, manage regulatory teams, and serve as a primary liaison with Health Authorities and internal stakeholders.
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.
Associate Director, Feasibility, Site Engagement and Strategic Planning & Operations, Malaysia & Singapore
BeiGene
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Full Time
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18 days ago
BeiGene
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 Senior Manager, Biostatistics performs scientific statistical analyses to support clinical trials and develops statistical analysis plans. They collaborate with cross-functional teams and manage vendors to ensure the quality and timeliness of deliverables.
Provide tactical financial support for Global Enabling Functions by tracking departmental spending and managing POs. Responsible for monthly close activities, quarterly forecasts, and annual budget cycles to improve spend transparency.
The Clinical Research Associate (CRA) executes clinical monitoring activities at trial sites and ensures compliance with ICH guidelines and GCP. They collaborate with the Regional Clinical Operations Manager to maintain study timelines and quality standards.
Associate Director, Clinical Supply Chain Sourcing Strategy and Innovation
BeiGene
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Full Time
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18 days ago
BeiGene
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.
The role is responsible for administering and supporting enterprise-wide learning platforms, including the LMS and BeOne University. Key duties include managing system configurations, triaging technical issues, and leading LMS-related projects to meet organizational training needs.
Senior Manager, Clinical Site Payments Processes and Systems
BeiGene
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Full Time
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20 days ago
BeiGene
Lead the development and governance of global clinical site payment processes, systems, and vendor platform configurations. Responsible for establishing metrics, training strategies, and ensuring financial compliance and audit readiness across internalized markets.
The role is responsible for ensuring clinical trial compliance at the country and site level using a risk-based approach. It involves overseeing GCP adherence, managing CAPAs, and supporting audit and inspection readiness to safeguard patient safety and data integrity.
Responsible for ensuring clinical trial compliance at the country and site level using a risk-based approach. The role involves managing compliance risks, overseeing site health checks, and supporting audit and inspection readiness.
Associate Director, Advanced Analytics, Patient Journey Insights and Predictive Modeling
BeiGene
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Full Time
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24 days ago
BeiGene
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.
Executive Director, Global Medical Affairs Companion Diagnostic Lead
BeiGene
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Full Time
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25 days ago
BeiGene
Develop and execute the Global Medical Affairs strategy for Companion Diagnostics (CDx) to support clinical and medical assets. Lead data generation efforts, engage oncology and pathology KOLs, and collaborate cross-functionally to ensure successful CDx launch and utilization.
The role serves as a strategic partner to the Head of Compliance, Americas, driving the execution and scalability of the North America Compliance Program. Key duties include managing compliance infrastructure, leveraging data analytics for risk mitigation, and leading cross-functional governance initiatives.
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.
The Director is responsible for developing and executing the promotional strategy for BRUKINSA, including product positioning and message development. This role involves collaborating with Sales and Business Analytics to optimize tactical plans and assess promotional effectiveness.
Lead the strategy and scaling of advanced analytics and AI-enabled solutions across Commercial, Medical Affairs, and Clinical Operations. Translate complex healthcare data into actionable insights to improve patient outcomes and operational performance.
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.
Account Manager, Solid Tumor - Little Rock, AR/Memphis, TN
BeiGene
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Full Time
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a month ago
BeiGene
The Account Manager promotes Solid Tumor products to physicians and healthcare professionals to increase patient access and usage. They are responsible for territory management, educating staff on product handling, and coordinating with market access and reimbursement teams.
The Key Account Manager is responsible for maximizing product sales and implementing marketing strategies within the Austrian hemato-oncology market. This includes providing scientific expert advice to hospital pharmacists and oncologists while managing regional sales goals and commercial projects.
Associate Director, Commercial Product Quality US Regional Lead, External Supply Quality
BeiGene
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Full Time
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a month ago
BeiGene
Lead the commercial product quality team to ensure externally manufactured products meet regulatory and company standards at CMOs. Oversee quality management processes, including change control, deviation handling, and inspection management for US regional supply.
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.
Associate Director, Strategic Planning and Operations, Office of the CMO, Solid Tumors
BeiGene
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Full Time
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a month ago
BeiGene
Support the business operations of the CMO office by managing budget, resource planning, and development prioritization. Lead continuous process improvements and standardization for Clinical Development in Solid Tumors while coordinating across multiple functional areas.
Director, Corporate Affairs and Communications, UK & Ireland
BeiGene
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Full Time
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a month ago
BeiGene
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.
The role provides administrative and project coordination support for medical processes, events, and projects in France. Key duties include managing budgets, coordinating vendor onboarding, and ensuring compliance and financial follow-up within local systems.
Executive Director, Global Medical Affairs Disease Area Lead, Solid Tumors
BeiGene
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Full Time
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a month ago
BeiGene
Lead the execution of Global Medical Affairs and Clinical Development strategies for gynecologic and other solid tumor programs. Oversee data generation, scientific communications, and the maintenance of global relationships with key opinion leaders.
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.
Responsible for developing and executing tactics for patient support programs, education, and promotions to drive growth for specific oncology products. This includes leading the lifecycle of promotional materials and collaborating cross-functionally to optimize patient access and experience.
Manager / Senior Manager, Global Category Lead, HR & Professional Services
BeiGene
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Full Time
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a month ago
BeiGene
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.
Associate Director, Direct-To-Consumer Innovation & Digital Health
BeiGene
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Full Time
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a month ago
BeiGene
Define and lead the strategy for next-generation customer experience technologies for patients and HCPs affected by hematologic malignancies. Partner with cross-functional teams to deliver scalable, compliant digital products and manage the CLL Navigator platform.
Senior Director, Global Commercial Logistics, Transportation, and Trade Compliance Manager
BeiGene
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Full Time
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2 months ago
BeiGene
Provide enterprise-wide strategic leadership for global supply chain operations, focusing on the end-to-end movement of goods and transportation network optimization. Lead global trade compliance programs to mitigate risk and ensure regulatory adherence across international borders.
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.
Lead the development and implementation of Strategic Business Plans for federal oncology accounts in the Northeast region. Collaborate cross-functionally to remove barriers to product access and nurture relationships with key VA/DoD stakeholders.
Lead the development and implementation of Strategic Business Plans for federal accounts including VA, DoD, and IHS. Collaborate cross-functionally to remove barriers to product access and nurture relationships with key oncology stakeholders.
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.
Executive Director, Enabling Functions Technology Solutions
BeiGene
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Full Time
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2 months ago
BeiGene
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.
The role involves line managing a team of Clinical Trial Management Associates, overseeing their professional development, and allocating resources to clinical research projects. Additionally, the manager provides operational support to cross-functional study teams from start-up through close-out, ensuring quality and compliance.
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.
Associate Director, Commercial Infrastructure & Operations
BeiGene
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Full Time
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2 months ago
BeiGene
Oversee the implementation and maintenance of commercial data platforms, including CRM and Business Intelligence, to drive operational excellence. Act as a key liaison between business stakeholders and technology teams to ensure high-quality, governed data for commercial analytics.
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.
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.
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.
Director, Head of Patient Recruitment and Retention, Americas
BeiGene
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Full Time
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2 months ago
BeiGene
Lead the design and execution of patient recruitment and retention strategies for oncology clinical trials across the Americas. Manage vendor partnerships, collaborate with patient advocacy groups, and oversee the implementation of patient-centric trial designs.
Head of Senior Director, Site Feasibility and Enablement, Americas
BeiGene
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Full Time
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2 months ago
BeiGene
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.
Associate Director, Program Management, North America GM Office
BeiGene
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Full Time
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2 months ago
BeiGene
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.
Oversee GMP and GDP operations for commercial products across European affiliates, ensuring compliance with EU and French regulations. Manage batch certification support, deviation management, and quality oversight of wholesalers and distributors.
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.
Associate Director, R&D Quality Good Pharmacovigilance Practice
BeiGene
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Full Time
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2 months ago
BeiGene
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.
Senior Director/Executive Director, Non-Personal Promotion Strategy and Execution
BeiGene
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Full Time
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2 months ago
BeiGene
Lead the non-personal promotion strategy and execution for the Hematology Franchise, managing digital presence across multiple brands. This includes owning digital media plans, managing agency relationships, and optimizing the omnichannel ecosystem to reach customers efficiently.
Develop and implement strategic business plans and market access contract pull-through strategies for regional oncology accounts. Build and maintain corporate relationships with C-suite executives and key stakeholders to remove barriers to product access.
Develop and implement strategic business plans and market access contract pull-through strategies for regional oncology accounts. Build and maintain corporate relationships with C-suite executives and key stakeholders to remove barriers to product access.
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.
Director, QMS BPO, Quality Issue Escalation, Risk & Knowledge Management
BeiGene
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Full Time
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2 months ago
BeiGene
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.
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.
Director, Program Management Office, Global Medical Affairs (ex-China)
BeiGene
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Full Time
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2 months ago
BeiGene
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.
Responsible for maximizing product sales and market share in the hematology and oncology sector within the assigned territory. This involves implementing commercial strategies, unlocking access barriers, and managing relationships with healthcare providers and stakeholders.
The MSL serves as the field-based representative for the Hematology therapeutic area, building professional relationships with HCPs and KOLs to exchange scientific information. They are responsible for collecting medical insights, supporting clinical trials, and collaborating with internal teams to execute medical affairs strategies.
Lead the strategy and implementation of AI and machine learning solutions to drive R&D digital transformation and operational efficiency. Partner with cross-functional stakeholders to identify high-impact use cases and deploy models that improve clinical data workflows and decision-making.
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.
Associate Director, AI Enablement (Commercial & Medical Affairs)
BeiGene
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Full Time
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2 months ago
BeiGene
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.
Manage strategic relationships with key regional clients to ensure timely access to innovative oncology therapies within public health institutions. Lead cross-functional teams to develop sustainable access strategies and communicate value propositions to key decision-makers.
Sales Representative (Chihuahua or Tijuana or Hermosillo)
BeiGene
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Full Time
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2 months ago
BeiGene
Responsible for maximizing product sales and implementing commercial strategies within the assigned territory to improve patient access. This includes managing medical visits, achieving KPIs, and building relationships with key opinion leaders in the healthcare system.
The MSL will act as a scientific expert to build relationships with opinion leaders and healthcare providers to support the Hematology-Oncology pipeline. They will coordinate external collaborations and disseminate scientific data to establish the company as a valued collaborator.
Responsible Pharmacist: Quality Assurance, Regulatory and QPPV β South Africa
BeiGene
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Full Time
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2 months ago
BeiGene
The Responsible Pharmacist manages regulatory affairs, quality assurance, and pharmacovigilance to ensure compliance with South African legislation. This includes overseeing product registrations, maintaining quality management systems, and acting as the Local QPPV for patient safety.
The Regional Manager will develop and execute regional plans, promote BeOneβs 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.
Lead the global commercial strategy and brand growth for TEVIMBRA across multiple solid tumor indications. Coordinate cross-functional teams to execute annual brand plans, operating plans, and long-range strategic goals.
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.
Manage and execute regulatory projects to secure and maintain market access for oncology products through all development phases. Lead strategic regulatory guidance, interface with Health Authorities, and oversee the preparation of global registration packages.
The Account Manager promotes Solid Tumor products to physicians and healthcare professionals to increase patient access and usage. They are responsible for territory management, educating staff on product handling, and coordinating with market access and reimbursement teams.
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.
Senior Director or Executive Director, Forecasting and Performance
BeiGene
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Full Time
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4 months ago
BeiGene
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 Director of Clinical Development will lead clinical program strategies and oversee the execution of clinical trials in partnership with internal and external stakeholders. They are responsible for authoring key clinical documents, managing study budgets, and providing scientific expertise throughout the drug development lifecycle.
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.
This senior strategic leader supports, influences, translates, and executes global oncology regulatory strategies across the entire drug development lifecycle, driving successful submissions and ensuring seamless cross-functional integration worldwide. The role involves proactively anticipating regulatory challenges, influencing decisions, and championing process improvements to secure on-time submissions and maintain market access.
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 role leads the development of Global Strategic Feasibility proposals, partnering closely with global program and study management teams for the design and delivery of clinical studies across all medicine development stages. The Lead ensures standardization of data and processes across regions to advise on quality decision-making and provides data-driven operational feasibility strategies for country selection, site allocation, and patient recruitment.
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.
Director, Global Value, Access & Pricing; Solid Tumors, Pipeline
BeiGene
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Full Time
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6 months ago
BeiGene
This role involves directing global strategies related to value, access, and pricing specifically for the solid tumors pipeline. The focus is on ensuring market success and appropriate reimbursement for pipeline assets in this therapeutic area.
The Business Operations Director is responsible for driving operational excellence and coordinating projects to optimize BeOneβs 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 BeOneβs 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.
The Associate Director will lead the global development of statistical programming projects and ensure the successful completion of programming deliverables. This includes collaborating with various teams, overseeing project resource planning, and contributing to regulatory submissions.
The Medical Director, Hematology will support clinical assets and pipeline by executing clinical development programs and deliverables in collaboration with various teams and external partners. The role includes generating and reviewing key clinical documents, providing scientific expertise, and ensuring compliance with regulatory requirements.