Job About the role • As the Environmental Health and Safety Manager, you will lead health and safety initiatives that ensure a safe workplace, uphold regulatory compliance, and support sustainable operations.
Job About the role • As the Environmental Health and Safety Manager, you will lead health and safety initiatives that ensure a safe workplace, uphold regulatory compliance, and support sustainable operations.
Anticipate and capitalize on emerging payer and societal needs Direct and oversee the co-development with Global Pricing, Value & Access (PVA) and cross-functional leaders to build compelling, evolving value narratives that impact payer decisions and drive optimal patient access worldwide • Drive strategic identification and prioritization of high-value opportunities—including new indications, lifecycle extensions, and innovative contracting models—across the portfolio Evidence Generation • Provide enterprise-wide vision and impactful leadership in evidence generation to secure HTA, payer, and market access objectives, integrating payer and real-world data needs across global, regional, and local programs Pioneer new approaches, including digital, data science, and AI, to transform evidence generation and proactively shape Takeda’s response to dynamic global value trends Review recommendations for advanced evidence needs (e.g., RWE, patient-centered outcomes), ensuring that internal and external partners are aligned to address emerging payer trends and requirements. • Lead the incorporation of innovative and payer-relevant endpoints in clinical development strategies and ensure robust HTA (including JCA) readiness HE and Value & Access Tools Set enterprise-wide benchmarks for scientific rigor in HEOR studies; ensure continuous innovation, external credibility, and differentiation with HTA bodies and payers • Drive the implementation of global HE strategies and tools (Value Platforms, Dossiers, value-based contract [VBC] toolkits) and ensure consistent capability build across regions and LOCs, directly spearheading global rollouts and advanced training programs Co-lead the conceptualization and execution of VBC options in collaboration with Market Access and Pricing, assessing and advancing their commercial impact Continuously advance all HE and Market Access tools in response to dynamic evidence and payer environments Market Access Serve as enterprise expert and spokesperson for Takeda’s global product value proposition—proactively engaging, influencing, and shaping both HTA policy and payer decisions to safeguard and expand market access opportunities Monitor and anticipate trends in the global HTA/reimbursement landscape to guide, shape, and transform Takeda’s HE and access strategies at the enterprise level Communication/Publication Elevate Takeda’s visibility and reputation through global HEOR communications, policy publications, and leading contributions to industry discourse • Lead global communication strategy, translating complex technical analyses into actionable, compelling value stories for executive, payer, and policymaker audiences Foster Superior Collaboration Mobilize, empower, and align cross-functional and external networks to deliver enterprise-wide HEOR and Market Access innovation. • Facilitate global knowledge sharing, mentoring, and continuous capability-building Cultivate and manage advanced collaborations with HE opinion leaders, vendors, and academic partners to ensure Takeda remains at the forefront of innovation and excellence in health economics Basic Qualifications • / Requirements Doctorate with 7+ years of experience, Master's with 9+ years of experience or Bachelor's with 12+ years of experience in healthcare industry with direct experience in global product value proposition development (industry or consulting) and interaction with payers, HTA bodies, relevant policymakers and strong patient-centered focus Robust understanding of the global payer environment and in-depth understanding of ex-US payer landscape including HTA trends and guidance (e.g., NICE, CADTH, PBAC, EU JCA), along with knowledge of US Medicare (Part D), ICER in the US and trends in Emerging Markets (e.g., China) – including reimbursement methodologies, pricing/reimbursement authorities’ decision-making process and current reimbursement issues • Strong knowledge and hands on experience in health economics, health technology assessment (HTA) tools, methods and filings, SLRs, ITCs, statistical analyses and economic modelling • Strong knowledge and understanding of clinical and epidemiological information, innovative global pricing models, all phases of drug development methods of analysis of large databases (e.g., claims data, electronic health records) and the major areas of Outcomes Research (PROs, modelling) Leadership – strong ability to work in a highly matrixed organization • Strong analytical capabilities and excellent communication skills (written and oral) Strategic thinking and demonstrated problem solving capability Influencing skills (one on one and in group setting) – consensus builder with ability to effective drive decision making Ability to translate technical issues to non-technical experts 5 to 10% Domestic and/or International travel may be required PREFERRED QUALIFICATIONS Previous experience in Hematology and/or Oncology A combination of in-depth knowledge of Global HTA (including EU JCA) requirements and direct experience in HTA submissions Direct payer experience and/or experience in Market Access Track record of peer-reviewed publications More about us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
Anticipate and capitalize on emerging payer and societal needs Direct and oversee the co-development with Global Pricing, Value & Access (PVA) and cross-functional leaders to build compelling, evolving value narratives that impact payer decisions and drive optimal patient access worldwide • Drive strategic identification and prioritization of high-value opportunities—including new indications, lifecycle extensions, and innovative contracting models—across the portfolio Evidence Generation • Provide enterprise-wide vision and impactful leadership in evidence generation to secure HTA, payer, and market access objectives, integrating payer and real-world data needs across global, regional, and local programs Pioneer new approaches, including digital, data science, and AI, to transform evidence generation and proactively shape Takeda’s response to dynamic global value trends Review recommendations for advanced evidence needs (e.g., RWE, patient-centered outcomes), ensuring that internal and external partners are aligned to address emerging payer trends and requirements. • Lead the incorporation of innovative and payer-relevant endpoints in clinical development strategies and ensure robust HTA (including JCA) readiness HE and Value & Access Tools Set enterprise-wide benchmarks for scientific rigor in HEOR studies; ensure continuous innovation, external credibility, and differentiation with HTA bodies and payers • Drive the implementation of global HE strategies and tools (Value Platforms, Dossiers, value-based contract [VBC] toolkits) and ensure consistent capability build across regions and LOCs, directly spearheading global rollouts and advanced training programs Co-lead the conceptualization and execution of VBC options in collaboration with Market Access and Pricing, assessing and advancing their commercial impact Continuously advance all HE and Market Access tools in response to dynamic evidence and payer environments Market Access Serve as enterprise expert and spokesperson for Takeda’s global product value proposition—proactively engaging, influencing, and shaping both HTA policy and payer decisions to safeguard and expand market access opportunities Monitor and anticipate trends in the global HTA/reimbursement landscape to guide, shape, and transform Takeda’s HE and access strategies at the enterprise level Communication/Publication Elevate Takeda’s visibility and reputation through global HEOR communications, policy publications, and leading contributions to industry discourse • Lead global communication strategy, translating complex technical analyses into actionable, compelling value stories for executive, payer, and policymaker audiences Foster Superior Collaboration Mobilize, empower, and align cross-functional and external networks to deliver enterprise-wide HEOR and Market Access innovation. • Facilitate global knowledge sharing, mentoring, and continuous capability-building Cultivate and manage advanced collaborations with HE opinion leaders, vendors, and academic partners to ensure Takeda remains at the forefront of innovation and excellence in health economics Basic Qualifications • / Requirements Doctorate with 7+ years of experience, Master's with 9+ years of experience or Bachelor's with 12+ years of experience in healthcare industry with direct experience in global product value proposition development (industry or consulting) and interaction with payers, HTA bodies, relevant policymakers and strong patient-centered focus Robust understanding of the global payer environment and in-depth understanding of ex-US payer landscape including HTA trends and guidance (e.g., NICE, CADTH, PBAC, EU JCA), along with knowledge of US Medicare (Part D), ICER in the US and trends in Emerging Markets (e.g., China) – including reimbursement methodologies, pricing/reimbursement authorities’ decision-making process and current reimbursement issues • Strong knowledge and hands on experience in health economics, health technology assessment (HTA) tools, methods and filings, SLRs, ITCs, statistical analyses and economic modelling • Strong knowledge and understanding of clinical and epidemiological information, innovative global pricing models, all phases of drug development methods of analysis of large databases (e.g., claims data, electronic health records) and the major areas of Outcomes Research (PROs, modelling) Leadership – strong ability to work in a highly matrixed organization • Strong analytical capabilities and excellent communication skills (written and oral) Strategic thinking and demonstrated problem solving capability Influencing skills (one on one and in group setting) – consensus builder with ability to effective drive decision making Ability to translate technical issues to non-technical experts 5 to 10% Domestic and/or International travel may be required PREFERRED QUALIFICATIONS Previous experience in Hematology and/or Oncology A combination of in-depth knowledge of Global HTA (including EU JCA) requirements and direct experience in HTA submissions Direct payer experience and/or experience in Market Access Track record of peer-reviewed publications More about us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
Accountabilities • Responsible for the development and finalization of study level contracts and change orders in partnership with key functions and aligned with Master Service Agreements, to ensure predictable delivery, quality and alignment to Takeda’s requirements, values and policies. • Lead ballparking, contracting and commercial management of complex clinical studies, understanding study requirements and translating into robust supplier contracts across a broad category of suppliers supporting R&D activities for assigned therapeutic areas and studies Apply appropriate commercial constructs, aligned to business requirements, to enable study start, even with evolving assumptions Utilize cost models and workbooks to validate contract pricing and budget assumptions for complex agreements and develop enhancements to improve validation capabilities • Drive negotiations with CRO’s and suppliers to secure optimal terms for Takeda • Manage contract amendments throughout the study lifecycle • Support study teams in completing final reconciliation at study closeout • Develop close collaborative working relationships with clinical operations and other key stakeholders to improve understanding and engagement Generate preliminary cost estimates to support Study Execution Teams (SET) in budget planning • Collaborate with study teams to address commercial/contractual challenges, proactively identify potential issues, develop contingency plans and escalate to Clinical • Partner Outsourcing/SPO leadership as necessary Escalate issues through the appropriate channels when local resolution is not achievable • Drive operational support & issue resolution by supporting teams in addressing operational and performance-related supplier issues • Ensure consistency between contractual agreement and operational implementation Serve as a SME and lead continuous improvement initiatives to enhance performance and efficiency, identify best practices through industry benchmarking.
Accountabilities • Responsible for the development and finalization of study level contracts and change orders in partnership with key functions and aligned with Master Service Agreements, to ensure predictable delivery, quality and alignment to Takeda’s requirements, values and policies. • Lead ballparking, contracting and commercial management of complex clinical studies, understanding study requirements and translating into robust supplier contracts across a broad category of suppliers supporting R&D activities for assigned therapeutic areas and studies Apply appropriate commercial constructs, aligned to business requirements, to enable study start, even with evolving assumptions Utilize cost models and workbooks to validate contract pricing and budget assumptions for complex agreements and develop enhancements to improve validation capabilities • Drive negotiations with CRO’s and suppliers to secure optimal terms for Takeda • Manage contract amendments throughout the study lifecycle • Support study teams in completing final reconciliation at study closeout • Develop close collaborative working relationships with clinical operations and other key stakeholders to improve understanding and engagement Generate preliminary cost estimates to support Study Execution Teams (SET) in budget planning • Collaborate with study teams to address commercial/contractual challenges, proactively identify potential issues, develop contingency plans and escalate to Clinical • Partner Outsourcing/SPO leadership as necessary Escalate issues through the appropriate channels when local resolution is not achievable • Drive operational support & issue resolution by supporting teams in addressing operational and performance-related supplier issues • Ensure consistency between contractual agreement and operational implementation Serve as a SME and lead continuous improvement initiatives to enhance performance and efficiency, identify best practices through industry benchmarking.
As an Associate Director, Scientific Training, Global Medical Affairs Oncology, you will: Be responsible for identification of learning needs, development and execution of strategic, tailored training plans and packages, and measurement of training success for Medical Affairs Scientific Training plans within GMAO, which includes ongoing needs assessments, developing and updating training programs, and establishing reinforcement training, including booster and focal training, to drive continual enhancement of GMAO scientific knowledge of Takeda Oncology marketed and pipeline products, relevant disease states, and competitor data • Ensure strategic collaboration with regions and countries to better understand training needs and deliver programs that meet these needs • Work with and oversee vendors to help support training initiatives.
As an Associate Director, Scientific Training, Global Medical Affairs Oncology, you will: Be responsible for identification of learning needs, development and execution of strategic, tailored training plans and packages, and measurement of training success for Medical Affairs Scientific Training plans within GMAO, which includes ongoing needs assessments, developing and updating training programs, and establishing reinforcement training, including booster and focal training, to drive continual enhancement of GMAO scientific knowledge of Takeda Oncology marketed and pipeline products, relevant disease states, and competitor data • Ensure strategic collaboration with regions and countries to better understand training needs and deliver programs that meet these needs • Work with and oversee vendors to help support training initiatives.
Job OBJECTIVES/PURPOSE The Finance Business Partner Lead is a seasoned finance professional that supports the Thousand Oaks Manufacturing site as the main business partner for the facility.
Job OBJECTIVES/PURPOSE The Finance Business Partner Lead is a seasoned finance professional that supports the Thousand Oaks Manufacturing site as the main business partner for the facility.
Job Lead, Global Pricing, Oncology (Associate Director) Takeda Pharmaceutical Cambridge, MA About the role • This role will lead the development of global pricing strategies and drive operational implementation across multiple launch and in-line assets for the Takeda Oncology Business Unit (OBU).
Job Lead, Global Pricing, Oncology (Associate Director) Takeda Pharmaceutical Cambridge, MA About the role • This role will lead the development of global pricing strategies and drive operational implementation across multiple launch and in-line assets for the Takeda Oncology Business Unit (OBU).
Job Associate Director, Consumer Marketing Takeda Pharmaceutical Cambridge, MA About the role • As the Associate Director of Consumer Marketing, you will be a champion of Takeda's culture and values while supporting the delivery of the consumer marketing strategic plan for a new product launch.
Job Associate Director, Consumer Marketing Takeda Pharmaceutical Cambridge, MA About the role • As the Associate Director of Consumer Marketing, you will be a champion of Takeda's culture and values while supporting the delivery of the consumer marketing strategic plan for a new product launch.
Job Associate Director, Consumer Marketing Takeda Pharmaceutical Cambridge, MA About the role • As the Associate Director of Consumer Marketing, you will be a champion of Takeda's culture and values while supporting the delivery of the consumer marketing strategic plan for a new product launch in Dermatology/Rheumatology.
Job Associate Director, Consumer Marketing Takeda Pharmaceutical Cambridge, MA About the role • As the Associate Director of Consumer Marketing, you will be a champion of Takeda's culture and values while supporting the delivery of the consumer marketing strategic plan for a new product launch in Dermatology/Rheumatology.
5–7+ years of experience in pharmaceutical/biopharma /healthcare marketing, communications, advertising • Experience working with promotional content and MLR review • Experience managing creation of HCP promotional materials Digital assets Sales rep materials Email / CRM content Websites or modular content • Strong project management, organizational, and communication skills. • Experience with budget management, vendor contracts, and financial oversight. • Experience submitting assets through Veeva Worked on MLR review cycles Managed digital and HCP promotional content production More about us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
5–7+ years of experience in pharmaceutical/biopharma /healthcare marketing, communications, advertising • Experience working with promotional content and MLR review • Experience managing creation of HCP promotional materials Digital assets Sales rep materials Email / CRM content Websites or modular content • Strong project management, organizational, and communication skills. • Experience with budget management, vendor contracts, and financial oversight. • Experience submitting assets through Veeva Worked on MLR review cycles Managed digital and HCP promotional content production More about us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
5–7+ years of experience in pharmaceutical/biopharma /healthcare marketing, communications, advertising • Experience working with promotional content and MLR review • Experience managing creation of HCP promotional materials Digital assets Sales rep materials Email / CRM content Websites or modular content • Strong project management, organizational, and communication skills. • Experience with budget management, vendor contracts, and financial oversight. • Experience submitting assets through Veeva Worked on MLR review cycles Managed digital and HCP promotional content production More about us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
5–7+ years of experience in pharmaceutical/biopharma /healthcare marketing, communications, advertising • Experience working with promotional content and MLR review • Experience managing creation of HCP promotional materials Digital assets Sales rep materials Email / CRM content Websites or modular content • Strong project management, organizational, and communication skills. • Experience with budget management, vendor contracts, and financial oversight. • Experience submitting assets through Veeva Worked on MLR review cycles Managed digital and HCP promotional content production More about us At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs.
Job • Purpose / Overview Takeda is seeking a strategic and execution-focused Change Management leader to drive adoption and value realization for the Labs of Tomorrow initiative across Research.
Job • Purpose / Overview Takeda is seeking a strategic and execution-focused Change Management leader to drive adoption and value realization for the Labs of Tomorrow initiative across Research.
Job Associate Director, Influencer & Social Media Marketing Takeda Pharmaceutical Cambridge, MA About the role • As the Associate Director of Influencer & Social Media Marketing, you will be a champion of Takeda's culture and values and will be responsible for building an industry leading influencer program for a new product launch in Dermatology that deepens patient engagement, builds trust in Takeda and elevates brand awareness.
Job Associate Director, Influencer & Social Media Marketing Takeda Pharmaceutical Cambridge, MA About the role • As the Associate Director of Influencer & Social Media Marketing, you will be a champion of Takeda's culture and values and will be responsible for building an industry leading influencer program for a new product launch in Dermatology that deepens patient engagement, builds trust in Takeda and elevates brand awareness.
How you will contribute Oversee and direct day-to-day and end-to-end operations across all PRAM functions (USRC, PromoMats, Print & Digital Asset Management, Material Distribution & Inventory Management, and PRAM Training), ensuring coordinated execution, cross-functional alignment, and consistent delivery of compliant and efficient processes. • Lead USRC Steering Committee governance, driving cross-functional alignment, decision-making, and oversight to ensure compliant, efficient, and predictable promotional review and approval processes. • Lead and operationalize PRAM support for US product launches and critical milestones, including PDUFA approval, Day 0 readiness, OPDP interactions, Form 2253 submissions, and end-to-end lifecycle activities (e.g., material approval, archival, and label change processes) to ensure timely, compliant execution.
How you will contribute Oversee and direct day-to-day and end-to-end operations across all PRAM functions (USRC, PromoMats, Print & Digital Asset Management, Material Distribution & Inventory Management, and PRAM Training), ensuring coordinated execution, cross-functional alignment, and consistent delivery of compliant and efficient processes. • Lead USRC Steering Committee governance, driving cross-functional alignment, decision-making, and oversight to ensure compliant, efficient, and predictable promotional review and approval processes. • Lead and operationalize PRAM support for US product launches and critical milestones, including PDUFA approval, Day 0 readiness, OPDP interactions, Form 2253 submissions, and end-to-end lifecycle activities (e.g., material approval, archival, and label change processes) to ensure timely, compliant execution.
POSITION ACCOUNTABILITIES • Lead delivery for one or more assets at GPT level or specialty area in preclinical, clinical, translational • Facilitate execution and delivery collaboration cross functionally in Global Project Teams (GPTs), generally within DQS and R&D, and with external vendors • Enable the consistent execution of the SQS and DQS seamless and predictable delivery mission • Lead and be accountable for asset level delivery strategies being implemented with effective risk identification and mitigation • Create an internal cross functional and external with vendors sphere of influence in predictable delivery • Identify opportunity for continuous improvement in delivery approaches and leverages fit-for-purpose mitigations by leveraging them EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS • Education: Must have degree in statistics/biostatistics or in other equivalent quantitative sciences along with the following specific credentials: PHD with ~ 5 years experience MS with ~ 8+ years experience Technical Skills Subject matter expertise in several quantitative and statistical areas and establishes oneself as a go-to colleague on a few topics Scientific understanding of drug R&D to inform methodological input with product team or in a platform • Strong communication skills and ability to translate effectively across functional lines Ability to • Identify and research new innovative approaches and leverage fit-for-purpose methods in to programs • Enable the tactical execution of the SQS and DQS vision and mission • Lead and be accountable for asset level strategies being implemented Demonstrate mentorship, matrix or direct management of small team of SQS colleagues • Facilitate collaboration cross functionally in GPTs and generally within DQS and R&D • Create an internal and external sphere of influence in area of expertise This position is currently classified as “ hybrid” in accordance with Takeda’s Hybrid and Remote • Work policy.
POSITION ACCOUNTABILITIES • Lead delivery for one or more assets at GPT level or specialty area in preclinical, clinical, translational • Facilitate execution and delivery collaboration cross functionally in Global Project Teams (GPTs), generally within DQS and R&D, and with external vendors • Enable the consistent execution of the SQS and DQS seamless and predictable delivery mission • Lead and be accountable for asset level delivery strategies being implemented with effective risk identification and mitigation • Create an internal cross functional and external with vendors sphere of influence in predictable delivery • Identify opportunity for continuous improvement in delivery approaches and leverages fit-for-purpose mitigations by leveraging them EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS • Education: Must have degree in statistics/biostatistics or in other equivalent quantitative sciences along with the following specific credentials: PHD with ~ 5 years experience MS with ~ 8+ years experience Technical Skills Subject matter expertise in several quantitative and statistical areas and establishes oneself as a go-to colleague on a few topics Scientific understanding of drug R&D to inform methodological input with product team or in a platform • Strong communication skills and ability to translate effectively across functional lines Ability to • Identify and research new innovative approaches and leverage fit-for-purpose methods in to programs • Enable the tactical execution of the SQS and DQS vision and mission • Lead and be accountable for asset level strategies being implemented Demonstrate mentorship, matrix or direct management of small team of SQS colleagues • Facilitate collaboration cross functionally in GPTs and generally within DQS and R&D • Create an internal and external sphere of influence in area of expertise This position is currently classified as “ hybrid” in accordance with Takeda’s Hybrid and Remote • Work policy.
POSITION ACCOUNTABILITIES • Lead delivery for one or more assets at GPT level or specialty area in preclinical, clinical, translational • Facilitate execution and delivery collaboration cross functionally in Global Project Teams (GPTs), generally within DQS and R&D, and with external vendors • Enable the consistent execution of the SQS and DQS seamless and predictable delivery mission • Lead and be accountable for asset level delivery strategies being implemented with effective risk identification and mitigation • Create an internal cross functional and external with vendors sphere of influence in predictable delivery • Identify opportunity for continuous improvement in delivery approaches and leverages fit-for-purpose mitigations by leveraging them EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS • Education: Must have degree in statistics/biostatistics or in other equivalent quantitative sciences along with the following specific credentials: PHD with ~ 5 years experience MS with ~ 8+ years experience Technical Skills Subject matter expertise in several quantitative and statistical areas and establishes oneself as a go-to colleague on a few topics Scientific understanding of drug R&D to inform methodological input with product team or in a platform • Strong communication skills and ability to translate effectively across functional lines Ability to • Identify and research new innovative approaches and leverage fit-for-purpose methods in to programs • Enable the tactical execution of the SQS and DQS vision and mission • Lead and be accountable for asset level strategies being implemented Demonstrate mentorship, matrix or direct management of small team of SQS colleagues • Facilitate collaboration cross functionally in GPTs and generally within DQS and R&D • Create an internal and external sphere of influence in area of expertise This position is currently classified as “hybrid” in accordance with Takeda’s Hybrid and Remote • Work policy.
POSITION ACCOUNTABILITIES • Lead delivery for one or more assets at GPT level or specialty area in preclinical, clinical, translational • Facilitate execution and delivery collaboration cross functionally in Global Project Teams (GPTs), generally within DQS and R&D, and with external vendors • Enable the consistent execution of the SQS and DQS seamless and predictable delivery mission • Lead and be accountable for asset level delivery strategies being implemented with effective risk identification and mitigation • Create an internal cross functional and external with vendors sphere of influence in predictable delivery • Identify opportunity for continuous improvement in delivery approaches and leverages fit-for-purpose mitigations by leveraging them EDUCATION, BEHAVIORAL COMPETENCIES AND SKILLS • Education: Must have degree in statistics/biostatistics or in other equivalent quantitative sciences along with the following specific credentials: PHD with ~ 5 years experience MS with ~ 8+ years experience Technical Skills Subject matter expertise in several quantitative and statistical areas and establishes oneself as a go-to colleague on a few topics Scientific understanding of drug R&D to inform methodological input with product team or in a platform • Strong communication skills and ability to translate effectively across functional lines Ability to • Identify and research new innovative approaches and leverage fit-for-purpose methods in to programs • Enable the tactical execution of the SQS and DQS vision and mission • Lead and be accountable for asset level strategies being implemented Demonstrate mentorship, matrix or direct management of small team of SQS colleagues • Facilitate collaboration cross functionally in GPTs and generally within DQS and R&D • Create an internal and external sphere of influence in area of expertise This position is currently classified as “hybrid” in accordance with Takeda’s Hybrid and Remote • Work policy.
Job About the role • Join Takeda as an Associate Director, Decision Science Center of Excellence where you lead brand-level promotional mix modeling and campaign lift assessment within the Decision Science team.
Job About the role • Join Takeda as an Associate Director, Decision Science Center of Excellence where you lead brand-level promotional mix modeling and campaign lift assessment within the Decision Science team.
Maintain trading partners and process rebates and fees within ModelN FLEX revenue management system for both Payer and GPO contracts. • Support data requests from US OBU Patient Value & Access field team, Distribution, Data Stewards, and IT, as well as external parties including Payers and GPOs.
Maintain trading partners and process rebates and fees within ModelN FLEX revenue management system for both Payer and GPO contracts. • Support data requests from US OBU Patient Value & Access field team, Distribution, Data Stewards, and IT, as well as external parties including Payers and GPOs.
Your prior experience in project management and technology transformation within the biopharma sector will be critical in ensuring successful project execution and adoption of new processes and technologies.
Your prior experience in project management and technology transformation within the biopharma sector will be critical in ensuring successful project execution and adoption of new processes and technologies.
Job • Reporting to the Head of E2E Process Reengineering, the Business Processes Transformation • Lead works with cross-functional teams across Takeda to analyze, design, implement, and monitor process improvements in key enterprise processes.
Job • Reporting to the Head of E2E Process Reengineering, the Business Processes Transformation • Lead works with cross-functional teams across Takeda to analyze, design, implement, and monitor process improvements in key enterprise processes.
Job ACCOUNTABILITIES Manage the digital dexterity pipeline Operate the platform-signal pipeline and standing cadence with DD (regular briefings for upcoming platform /tool changes and roadmap timing).
Job ACCOUNTABILITIES Manage the digital dexterity pipeline Operate the platform-signal pipeline and standing cadence with DD (regular briefings for upcoming platform /tool changes and roadmap timing).