Senior Manager, R&D Asset Transition & Integration Office (RATIO)

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 About the role:  At Takeda, we are guided by our purpose of Better Health for People, Brighter Future for the World and our commitment to patients, our people and the planet. As we continue to evolve our portfolio through acquisitions, partnerships, and divestitures, the ability to transition and integrate assets seamlessly is essential to delivering on our commitments to patients, regulators, and partners.    We are seeking a Senior Manager to join the R&D Asset Transition & Integration Office (RATIO), the function responsible for executing R&D asset transitions across integrations, in-licensing, asset wind-downs, divestments, and externalizations. In this role you will support and lead selective transitions and manage delivery across the R&D functions to a clean, compliant asset close.  You will operate at the intersection of science, operations, and strategy—bringing structure to complex transitions while maintaining the highest standards of quality and data integrity.    How you will contribute: As a transition lead within RATIO, you will:  Support or selectively lead R&D asset transitions (particularly wind-downs or terminations), defining scope, sequencing, critical path, resourcing, and target end state  Translate contractual obligations—license agreements, transition plans, and post-term commitments—into executable operational workplans with named owners and dates  Coordinate delivery across Regulatory Affairs, Pharmacovigilance, Clinical Operations, Clinical Data Management, Biostatistics, Pharmaceutical Sciences, Nonclinical, Quality, Procurement, Legal, Finance, and Data & Technology  Work with R&D functions to manage study closeout, sample and material disposition, regulatory withdrawal, trial transparency obligations, and financial reconciliation   Support governance cadence for assigned transitions; escalate with clear recommendations and present to senior leadership forums  Execute critical transition activities, such as data and records transfer, regulatory filing transitions, safety and pharmacovigilance handovers, system migrations and decommissioning, and contract and vendor transitions  Track and report ongoing post-term commitments, ensuring obligations to partners and health authorities are met  Contribute to RATIO frameworks, playbooks and tools, incorporating lessons learned so that each transition is more efficient than the last    What Makes This Role Unique:  This role is part of an innovative capability that is leading across the pharma and CRO industry. Accordingly, you’ll be close to some of the most complex and high-impact work in R&D. You will:  Own transitions that directly shape Takeda's R&D portfolio, with visibility to senior leadership  Work across the full breadth of R&D functions rather than within a single discipline  Bring clarity and structure to ambiguity, often where no established precedent exists  Represent Takeda operationally to external partners and counterparties    Success in this role requires someone who has a learning mindset, balances operational rigor with judgement, and drives alignment across a highly matrixed, global environment.    What You Bring:  Working knowledge of R&D processes, such as clinical development, regulatory, safety, and quality systems  Experience in program management through complex or multi-functional initiatives    Understanding of data and records management, such as regulatory data transfer, system transitions, and archival strategies  Familiarity with global R&D systems and infrastructure, and how they interact during transitions  Strong communication and interpersonal skills and ability to drive a collaborative environment  Ability to navigate ambiguity and drive progress, even in highly complex environments    Minimum Requirements/Qualifications: Minimum Bachelor's degree in a scientific or related field required; advanced degree welcomed  6+ years of relevant experience in the pharmaceutical or biotech industry, particularly in R&D strategy and operations and/or program management  Demonstrated delivery in global matrixed environments  Experience working with external counterparties—partners, licensors, CROs, or vendors  Fluent English at a level suitable for global governance forums    Preferred:  Experience in any of the following: R&D alliance management, Business Development (e.g., M&A integration, divestment, in-licensing), R&D technology or sponsor transfer, asset termination, or Life Sciences Strategy or Management Consulting  Contract literacy  Budget forecasting, tracking and closeout for program spend  Experience working across cultures and time zones    Additional Information:  May require travel, including international travel  This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy    More about us: At Takeda, we are transforming patient care through the development of novel specialty pharmaceuticals and best in class patient support programs. Takeda is a patient-focused company that will inspire and empower you to grow through life-changing work. Certified as a Global Top Employer, Takeda offers stimulating careers, encourages innovation, and strives for excellence in everything we do. We foster an inclusive, collaborative workplace, in which our teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. This position is currently classified as "hybrid" following Takeda's Hybrid and Remote Work policy. #LI-Hybrid #LI-AA1 Locations Warsaw, Poland Worker Type Employee Worker Sub-Type Regular Time Type Full time