Takeda Pharmaceutical

Lead supplier governance and operational excellence for strategic suppliers supporting clinical studies, driving cost optimization, process standardization, and compliance. | Requires 15+ years in process improvement, business operations, procurement enablement, or project management in clinical development, with strong financial, negotiation, and supplier governance skills. | By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Are you looking for a patient-focused, innovation-driven company to inspire you and empower you to shine? Join us as the Sr. Director, Supplier Relationship Management (FSP) based in Cambridge, MA reporting to the Head Partnership Health and Supplier Management. Objective / Purpose: Reporting to the Head of SPO, the Sr Director, Supplier Relationship Management (FSP) is responsible for driving operational and commercial excellence with key strategic FSP suppliers supporting Takeda’s R&D portfolio. This role ensures strong FSP executive and operational governance, FSP operational strategies, cost optimization, and continuous improvement while managing the global enterprise relationship across all clinical studies and activities. Accountabilities: • Build lead and oversee the supplier governance framework, including chairing governance meetings and maintaining critical oversight tools (e.g performance metrics, scorecards, risk registers) • Drive operational performance improvements by conducting thorough root cause analysis, implementing corrective actions, incorporating "shift-left" strategies, and driving process standardization. • Collaborate with business functions to ensure operational delivery is in line with commercial constructs and operational performance targets, driving continuous improvement • Partner with Procurement and key stakeholders to drive robust category strategies, update and oversee Master Service Agreements (MSA) and to define and implement commercial constructs supporting strategic initiatives • Ensure that operational and commercial changes are standardized and incorporated into ways of working and supporting commercial constructs e.g., MSA, SOW, cost workbook, gain-share commercial constructs • Work with suppliers to incorporate additional content, pricing, definitions, and strategic initiatives into cost workbooks • Lead and prioritize supplier-focused Value Analysis/Value Engineering (VA/VE) activities, innovation councils, and cost optimization efforts • Ensure supplier innovation and continuous improvement initiatives align with business objectives and sourcing strategies • Work closely with Procurement, Therapeutic Areas, Business Partners, CPO and Study teams to review and drive sourcing strategies • Develop and monitor operational performance metrics and insights, collaborating with the Enablement Team to drive data-driven decision making • Partner with Therapeutic Area (TA) Business Partners to drive process and policy optimization within TAs. • Work closely with the Enablement Team to ensure consistent adoption of best practices and knowledge sharing. • Foster a culture of continuous improvement by identifying and implementing process improvements and innovative solutions. • Foster strong industry collaborations to ensure continuous exchange of innovative ideas and best practices • Ensure compliance with all applicable internal policies and procedures, regulations; support inspection readiness of all regulated activities. Education & Competencies (Technical and Behavioral): • BS/BA required; advanced technical degree preferred • 15+ years of experience in process improvement, business operations, procurement enablement, or project management in a clinical development environment • Exceptional supplier relationship and governance skills • Strong financial and commercial management • Experience leading value-driven initiatives, including Value Analysis/Value Engineering and cost optimization, implementation of supplier development programs • Ability to translate complex problems into clear, actionable solutions • Highly skilled in leveraging data insights for decision-making and process optimization • Strong financial management, negotiation and conflict resolution and team building skills. • Excellent communication and interpersonal skills • Strong understanding of GCP, ICH guidelines, and clinical trial regulations Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: Boston, MA U.S. Base Salary Range: $208,200.00 - $327,140.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations Boston, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time Job Exempt Yes It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Lead oncology drug discovery programs from discovery to clinic, set strategic vision, manage cross-functional teams, and represent Takeda externally. | PhD in life sciences with 15+ years in drug discovery and preclinical development, 10+ years in scientific leadership, proven track record advancing oncology programs to IND, and strong leadership and communication skills. | By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge. Job Description Global Therapeutic Research Lead, Oncology Are you a biotech or pharma executive ready to shape the future of oncology drug discovery? Join Takeda’s ODDU Leadership Team to drive AI-powered innovation and deliver transformative medicines to patients worldwide. As a member of the Oncology Drug Discovery Unit (ODDU) Leadership Team, you will set the vision for next-generation oncology discovery, lead high-impact project teams, and represent Takeda at the highest levels—internally and externally. You will champion the integration of AI/ML-driven approaches and future-forward ways of working, ensuring ODDU remains at the forefront of scientific innovation and patient impact. Key Responsibilities and Accountabilities • Leveraging a proven track record of leading discovery programs to clinic, the Global Therapeutic Research Lead (GTRL) is a pipeline critical strategic leader responsible for driving Research’s most promising projects to the clinic, taking responsibility for the asset strategy and serving as the cross-functional team leader. • As member of the ODDU Leadership Team, this leader will help guide and execute the vision and strategy for the ODDU, leveraging AI/ML and digital innovation to accelerate discovery and development. • As a key ‘drug hunter’ talent in Takeda Research, this leader will take on key mentoring roles, including helping to develop the next generation of project team leaders. This leader will also play a visible role in global Research initiatives. • Driven by a passion for making a difference for patients, this leader will play a critical role in accelerating transformative drug discovery to deliver life-changing therapies to patients with rigor and urgency. Serve as a visible leader and ambassador for Takeda, representing the organization with external partners, at scientific conferences, and in industry forums. Who You Are • Visionary leader with a track record as an experienced ‘drug hunter’ in biotech or large pharma. • Ph.D. or equivalent in life sciences; 15+ years of experience in drug discovery and preclinical development. • Proven ability to advance programs from discovery to IND and beyond, with major contributions to at least 3 INDs. • Deep expertise in oncology and broad experience across multiple therapeutic areas. • Recognized for building high-performing teams, driving innovation, and delivering results in complex, matrixed environments. • Passionate about emerging technologies and AI/ML-driven drug discovery. • Outstanding communicator and external influencer. Program & Portfolio Leadership • Oversee drug discovery and development programs across building a connected view of the project disease area strategy and treatment paradigm and can represent all core expertise at depth and align with stakeholders and sponsors across the organization including Research, Clinical Development and Commercial stakeholders and executive level governance committees. • Advance promising molecules—engineered by AI/ML-driven platforms—through development candidate stage gates, lead IND-enabling activities, and partner with clinical organizations to deliver differentiated therapeutics into the clinic. • GTRLs are responsible for creating the medicine vision, early asset strategy and managing multiple external partnerships that accelerate delivery of the project in partnership with a Global Project Lead following Candidate Selection. • GTRLs will establish smart, fast, and critical path minded practices for groups, including integrating new strategies and competitive industry ways of working. • GTRL will advise on the continuous infusion of new Research projects aligned to strategy to generate a sustainable Research Engine generating a steady flow of high-quality INDs every year. Cross-Functional & External Collaboration • Drive cross-functional collaboration with Protein Sciences, Early-stage Biology, Therapeutic Assay Sciences, and Clinical Development. Build and maintain relationships with key stakeholders, including academic institutions, research organizations, and industry partners. Represent ODDU and Takeda externally, serving as an ambassador for scientific and business development. Accountabilities • Drive the end-to-end drug discovery process for high-priority oncology programs, from target identification through preclinical development and IND submission. • Shape and communicate program strategy, ensuring alignment with internal and external stakeholders. • Mentor and develop future leaders, elevating the organization’s scientific and operational capabilities. • Ensure scientific excellence, operational rigor, and a culture of innovation across all programs. • Represent ODDU and Takeda in high-level governance, external collaborations, and business development opportunities. Education & Competencies (Technical and Behavioral): • Ph.D. or equivalent in life sciences; 15+ years of experience in drug discovery and preclinical development, with 10+ years in scientific leadership roles. • Proven track record of advancing oncology programs from discovery to IND and beyond, with major contributions to at least 3 INDs. • Deep expertise in oncology and broad experience across multiple therapeutic areas. • Demonstrated ability to build and lead high-performing teams, drive innovation, and deliver results in complex, matrixed environments. • Outstanding communication, external influence, and partnership-building skills. Takeda Compensation and Benefits Summary We understand compensation is an important factor as you consider the next step in your career. We are committed to equitable pay for all employees, and we strive to be more transparent with our pay practices. For Location: Boston, MA U.S. Base Salary Range: $208,200.00 - $327,140.00 The estimated salary range reflects an anticipated range for this position. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job. The actual base salary offered will be in accordance with state or local minimum wage requirements for the job location. U.S. based employees may be eligible for short-term and/ or long-term incentives. U.S. based employees may be eligible to participate in medical, dental, vision insurance, a 401(k) plan and company match, short-term and long-term disability coverage, basic life insurance, a tuition reimbursement program, paid volunteer time off, company holidays, and well-being benefits, among others. U.S. based employees are also eligible to receive, per calendar year, up to 80 hours of sick time, and new hires are eligible to accrue up to 120 hours of paid vacation. EEO Statement Takeda is proud in its commitment to creating a diverse workforce and providing equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, gender expression, parental status, national origin, age, disability, citizenship status, genetic information or characteristics, marital status, status as a Vietnam era veteran, special disabled veteran, or other protected veteran in accordance with applicable federal, state and local laws, and any other characteristic protected by law. Locations Boston, MA Worker Type Employee Worker Sub-Type Regular Time Type Full time Job Exempt Yes It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.