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.
BeiGene
152 Remote Job Openings at BeiGene
Responsible for ensuring robust 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. It involves overseeing GCP adherence, managing CAPAs, and supporting audit and inspection readiness to safeguard patient safety and data integrity.
Associate Director, Advanced Analytics, Patient Journey Insights and Predictive Modeling
BeiGene
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Full Time
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4 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.
Oversee global safety operations, including the collection, processing, and reporting of ICSRs and safety activities in clinical trials. Lead the Global Patient Safety operational technology strategy and manage safety operations specifically for the China market.
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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5 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.
Accountable for regional clinical study delivery, ensuring inspection readiness, quality, and adherence to timelines and budgets. Leads regional clinical operations teams and external vendors while collaborating with global stakeholders to align regional deliverables with study goals.
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.
The Senior Manager, Safety Epidemiologist executes data analyses and interprets studies to inform the natural history of disease and safety risk management. They contribute to regulatory safety reports and author epidemiological publications to support product differentiation.
Supervises clinical data publication and transparency compliance across the study portfolio in accordance with international regulations. Manages a team of direct reports, oversees resource planning, and directs the implementation of disclosure strategies and processes.
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.
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.
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.
Accountable for the global delivery of oncology clinical studies within agreed timelines, budgets, and quality standards. Leads cross-functional study teams and manages external vendors to ensure inspection readiness and alignment with corporate goals.
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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11 days 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.
The Contract Manager oversees the administration, negotiation, and execution of clinical site contracts to ensure they meet timelines and regulatory requirements. They serve as the primary point of contact for clinical operations and legal teams while managing site budgets and Fair Market Value compliance.
Associate Director, Commercial Product Quality US Regional Lead, External Supply Quality
BeiGene
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Full Time
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12 days 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.
The Associate Product Manager supports marketing engagement efforts in Germany by implementing tactics aligned with product strategies and brand priorities. This includes managing KOL relationships, coordinating congress logistics, and collaborating cross-functionally to prepare for product launches.
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.
The Contract Manager oversees the administration, negotiation, and execution of clinical site contracts to ensure they meet timelines and regulatory requirements. They serve as the primary point of contact for clinical operations and legal teams while managing site budgets and Fair Market Value standards.
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.
Manages drug supply activities including planning, labeling, and distribution for clinical studies to ensure continuous patient supply. Oversees relationships with external supply partners and implements process improvements within a cGMP environment.
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.
Responsible for the planning and execution of global distribution for finished products and active ingredients, ensuring legal and regulatory compliance. The role involves managing logistics budgets, overseeing courier vendors, and collaborating cross-functionally to optimize the supply chain for patient delivery.
Associate Director, Strategic Planning and Operations, Office of the CMO, Solid Tumors
BeiGene
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Full Time
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18 days 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.
Lead and oversee a team of Product Safety Physician Leads to establish strategic safety direction across a specific franchise or disease area. Accountable for safety oversight of all compounds, including shaping portfolio-level strategies and representing Safety Science in governance forums.
Director, Corporate Affairs and Communications, UK & Ireland
BeiGene
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Full Time
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18 days 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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20 days 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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21 days 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.
Define and execute a comprehensive enterprise-wide AI and data strategy to transform the organization into a data-driven enterprise. Lead the development of AI tools and foster a culture of innovation while mentoring high-performing technical teams.
Associate Director, Direct-To-Consumer Innovation & Digital Health
BeiGene
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Full Time
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24 days 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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25 days 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.
Develop and implement statistical analysis plans (SAP) for clinical study reports and health authority submissions. Collaborate with cross-functional teams to design clinical trials and analyze data for hematology studies.
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 accounts including VA, DoD, and IHS. Collaborate cross-functionally to remove barriers to product access and nurture relationships with key oncology stakeholders.
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.
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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a month 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.
Perform medical review of Individual Case Safety Reports (ICSRs) to determine event seriousness, expectedness, and causality. Identify potential safety signals and contribute to aggregate safety analysis for regulatory submissions.
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.
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.
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.
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.
Associate Director, Commercial Infrastructure & Operations
BeiGene
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Full Time
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a month 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.
Director, Head of Patient Recruitment and Retention, Americas
BeiGene
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Full Time
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a month 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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a month 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.
Define and scale enterprise tagging, taxonomy, and content measurement capabilities across Commercial and Medical omnichannel ecosystems. Act as the technical authority for structuring content and campaigns to ensure data quality and interoperability for global reporting.
Lead regional strategic feasibility efforts to deliver data-driven reports for early to late-stage medicine development. Coordinate site identification, recruitment strategies, and enrollment forecasting in collaboration with global teams and stakeholders.
Associate Director, Program Management, North America GM Office
BeiGene
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Full Time
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a month 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.
Associate Director, R&D Quality Good Pharmacovigilance Practice
BeiGene
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Full Time
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a month 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.
Serve as a strategic analytics partner to support the launch and growth of BEQALZI and BTK CDAC by generating actionable insights. Lead analytics across commercial performance, customer segmentation, and market dynamics to inform critical business decisions.
The Marketing Lead is responsible for the strategic and operational implementation of product management for the oncology portfolio in Israel. This includes developing omnichannel engagement strategies, managing brand positioning, and collaborating with cross-functional teams to ensure patient access.
The Associate Director provides strategic ownership and optimization of enterprise content platforms, specifically Veeva Vault PromoMats and MedComms. The role focuses on streamlining PRC/MRC review processes, driving modular content adoption, and integrating AI capabilities to improve content lifecycle efficiency.
Senior Director/Executive Director, Non-Personal Promotion Strategy and Execution
BeiGene
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Full Time
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a month 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.
The Director of Clinical Development will lead the execution of clinical programs and medical assets, focusing on strategy development and the creation of key clinical documents. They will collaborate with internal teams and external partners to ensure studies are delivered within scope, budget, and timelines.
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.
Accountable for regional clinical study delivery, ensuring quality, inspection readiness, and adherence to timelines and budgets. Leads regional operations teams and external vendors while collaborating with global stakeholders to align regional deliverables with study goals.
Manage local pharmaceutical affairs, including regulatory and quality assurance operations, acting as a contact for competent authorities in Germany. Oversee GxP governance, product labeling, distribution activities, and the review of promotional materials.
Responsible for processing vendor and employee payments across EMEA and US entities while ensuring compliance with company policies. The role involves managing payment runs, coordinating with Treasury and Procurement, and maintaining accurate vendor master data.
Director, QMS BPO, Quality Issue Escalation, Risk & Knowledge Management
BeiGene
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Full Time
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a month 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.
Key Account Manager Solid Tumor - Dresden, Chemnitz, Cottbus
BeiGene
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Full Time
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a month ago
BeiGene
The Key Account Manager is responsible for maximizing product sales and implementing marketing strategies within the served territory to achieve defined targets. This includes providing scientific expert advice to hospital pharmacists and oncologists while managing commercial projects to optimize patient care.
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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a month 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.
Lead and manage clinical supply chain activities, overseeing demand and supply plans to ensure continuous patient supply while minimizing waste. Manage direct reports and collaborate with internal stakeholders like Clinical Operations and Regulatory Affairs to align organizational goals.
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.
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.
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 also involves mentoring other medical writers and leading the optimization of departmental processes and templates.
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.
Lead the delivery of an aligned People strategy for Germany, focusing on organizational design, talent management, and employee experience. Act as a strategic HR coach to leadership and ensure compliance with German labor laws and works council requirements.
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.
Develop and execute marketing strategies for the BeOne portfolio in Mexico to ensure patient access to medicines. Collaborate with cross-functional teams to translate regional strategies into operational tactics and manage the commercial budget.
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.
Responsible Pharmacist: Quality Assurance, Regulatory and QPPV – 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 BeOne’s products, and provide education to healthcare professionals. They will also ensure compliance with laws and regulations while managing administrative functions.
Lead and mentor a regional team of clinical study managers to ensure the timely and high-quality delivery of clinical trials. Drive the regional clinical operations strategy, manage resourcing, and collaborate with global stakeholders to meet business goals.
Senior Director, Clinical Supply Agreement Contract Management & Alliance Management
BeiGene
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Full Time
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2 months ago
BeiGene
Lead the execution and management of Clinical Supply Agreements (CSA) and collaborations with external industry partners. Oversee end-to-end contract management, ensuring operational feasibility, compliance, and alignment with company strategy.
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.
Associate Manager, Regional Business & Operations Support
BeiGene
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Full Time
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2 months ago
BeiGene
The Associate Manager provides regional enablement and business operations support to GCO JAPAC, focusing on day-to-day business rhythm, metrics, reporting, and process standardization. This role also involves operational support for clinical trial planning and improving visibility and consistency across regional priorities.
Develop and execute the global Medical Affairs training strategy for the hematology franchise to build deep scientific expertise. Lead the creation of application-based learning experiences, onboarding certifications, and field medical resources across global regions.
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.
The role serves as the primary owner of contract operations and onboarding for the market access team. It involves managing large-scale events, congress planning, and coordinating communications and administrative processes across various functions.
Oversees clinical monitoring activities and manages the CRA team to ensure compliance with ICH-GCP and company SOPs. Leads resource allocation, performance management, and strategic initiatives to optimize clinical operations and trial delivery.
The Senior Associate plans and executes U.S. regulatory submissions (IND, NDA, BLA) to the FDA, ensuring accuracy and compliance. They serve as the primary operational liaison between regulatory strategy, publishing, and cross-functional stakeholders to meet strict deadlines.
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.
Senior Regional Director, Medical Value and Outcomes (US Lead)
BeiGene
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Full Time
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2 months ago
BeiGene
Lead and manage the US Field Based Medical Value and Outcomes team to disseminate clinical and health-economic data to healthcare decision makers. Act as a key connector between field medical, HEOR, market access, and commercial leadership to ensure consistent value narratives.
Regional Manager, Hematology (Canada - Alberta & Saskatchewan))
BeiGene
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Full Time
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2 months ago
BeiGene
The Regional Manager is responsible for driving the use of Brukinsa by building trusted partnerships with healthcare practitioners and stakeholders in Alberta and Saskatchewan. They will execute regional business plans and provide scientific expertise to improve cancer patient outcomes.
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.
Field Medical Director, Solid Tumor- Breast and Lung Boston/New England
BeiGene
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Full Time
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2 months ago
BeiGene
The Field Medical Director coordinates external collaborations and research with healthcare providers to support the solid tumor pipeline. They develop regional strategies to maintain compliant relationships with opinion leaders and provide medical affairs support for pre- and post-launch assets.
The intern will support Regulatory Affairs CMC projects by maintaining accurate information in the RIM system and assisting with data remediation. They will also contribute to the drafting of CTD CMC sections for global health authority submissions.
The Senior Manager will design and execute global market research projects to influence commercialization strategies for the oncology portfolio. This includes translating research into actionable insights and collaborating with cross-functional partners to address key strategic business objectives.
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.
Senior Associate, Regulatory Affairs, Promotional Operations
BeiGene
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Full Time
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2 months ago
BeiGene
Responsible for coordinating the processing and review of promotional materials through the Promotional Review Committee and document management systems. Supports the preparation of regulatory submissions for advertising materials in accordance with FDA requirements.
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.
Senior Manager Treasury Solutions, Finance Technology Solutions
BeiGene
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Full Time
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2 months ago
BeiGene
The Senior Manager, Treasury Solutions will lead the support, sustainment, and growth of Treasury and Cash Management capabilities within SAP. They will act as the primary solution architect and manager, partnering with business stakeholders to develop roadmaps and implement strategic initiatives.
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 Associate Director will serve as the operational hub connecting Business Development, Regulatory, Finance, and Governance to support external partnership models. Key duties include managing intake and triage, resource forecasting, governance coordination, and providing project management support for complex engagements.
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.
Associate Director, Digital Quality Management Systems, Change Management and Digital Adoption
BeiGene
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Full Time
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3 months ago
BeiGene
The Associate Director will facilitate the adoption of digital quality tools and serve as the Business Process Owner for AI capabilities within Global Quality. This role involves developing communication strategies, designing training programs, and driving cross-functional alignment on AI governance and standards.
The Associate Director is responsible for developing and executing customer strategies for Key Opinion Leaders (KOLs) to support the hematology oncology portfolio. This role involves collaborating with cross-functional teams to drive commercial strategy, manage promotional activities, and communicate market insights.
Senior Director or Executive Director, Forecasting and Performance
BeiGene
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Full Time
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3 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.
Senior Manager, Digital Health: Project Management & Operations
BeiGene
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Full Time
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3 months ago
BeiGene
The Senior Manager will serve as the operational backbone for the Digital Health team, managing a portfolio of projects including digital strategy, platforms, and clinical trials. They are responsible for designing scalable project management infrastructure, driving cross-functional alignment, and overseeing day-to-day operational functions like budget tracking and vendor management.
This role is responsible for the effective management of all aspects of Investigator-initiated Trials (IITs), including implementation across multi-institutions in compliance with regulations and assisting with program management tasks like contract tracking and report creation. Essential functions include supporting IIT operations, leading the Medical Internal Review Committee (MIRC), serving as a main point of contact for research teams, and coordinating study budgets and payments.
The Associate Director will ensure excellence and innovation in delivering cross-functional Customer Engagement, focusing on patient access to products by assessing needs and executing upskilling activities for the German team. This role involves driving business decisions centered on patient care and supporting integrated launch plans and field performance across the region.
The role involves designing, planning, and leading statistical analyses for Real-World Data (RWD) and Real-World Evidence (RWE) studies, including comparative effectiveness and safety assessments. Responsibilities also include overseeing and validating statistical programming deliverables, performing analyses in big data environments, and applying AI capabilities to enhance workflows.
The Marketing Director is responsible for building and leading the marketing function to develop and execute commercialization strategies for existing and future Haematology products in the UK and Ireland. This includes overseeing overall strategy, tactical plans, collaborating with cross-functional leaders, and managing the marketing team's coaching and development.
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.
The Medical Science Liaison (MSL) is responsible for building professional relationships with external medical community stakeholders to exchange scientific information regarding the company's therapeutic areas and pipeline. This role involves collecting, analyzing, and communicating actionable medical insights, emerging trends, and unmet medical needs to internal teams while ensuring regulatory and ethical compliance.
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.
The Sales Director Benelux is responsible for driving commercial performance across Belgium, the Netherlands, and Luxembourg by leading the sales force, ensuring effective execution of brand strategies, and maximizing value through stakeholder engagement and cross-functional collaboration. Key functions include developing and implementing the Benelux sales strategy, managing performance metrics, leading and developing the KAM team, and overseeing sector/account planning excellence.
The Associate Director, Regulatory Affairs CMC, is responsible for developing and implementing global regulatory CMC strategies to secure and maintain market access for assigned products in coordination with internal stakeholders. This role involves managing regulatory CMC aspects for large molecules through all development phases, post-approval, and lifecycle stages, primarily focusing on creating regulatory strategies for submissions.
Director, Global Value, Access & Pricing; Solid Tumors, Pipeline
BeiGene
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Full Time
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5 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 BeOne’s in-market portfolio performance. This includes overseeing operational planning, managing resources, and ensuring effective execution of initiatives.
The Associate Director will lead the strategic growth and operational excellence of SAP Finance capabilities for BeOne’s EMEA operations. This includes defining the global vision for SAP Finance solutions and ensuring compliance with local statutory requirements.
The Director, Global Regulatory Lead develops, implements, and advises on global regulatory strategies to secure and maintain market access for products in alignment with business objectives. This role manages regulatory aspects through all development phases, post-approval, and life-cycle, providing strategic oversight and acting as an advisor/liaison to global project teams.
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 GCO Program Lead is accountable for strategic operational planning and clinical operational performance of designated programs. This role includes leading the global team, overseeing project delivery, and collaborating with other program leads to ensure execution excellence.
Lead the Central Statistical Monitoring team to support risk-based quality management in clinical trials. Develop statistical monitoring indicators and models, ensuring data integrity and subject safety.
Associate Director, Biostatistics (Central Statistical Monitoring)
BeiGene
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Full Time
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6 months ago
BeiGene
Lead the Central Statistical Monitoring team to support risk-based quality management in clinical trials. Develop statistical monitoring indicators and models, ensuring data integrity and subject safety.
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.
