Sr. Manager, Medical Review - GCM

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 Role Objectives: • Provide Medical and scientific review expertise across MLR and cMLR processes, ensuring content is scientifically accurate, balanced, evidence-based, compliant, and aligned with approved data, product information, and scientific evidence in the literature. •       Serve as a key Medical reviewer and scientific advisor to content-development, Medical Communications, Congress, and Content Factory teams, enabling the development of high-quality, review-ready content and efficient approval pathways. •       Partner with Medical, Regulatory, Legal, Compliance, and cross-functional stakeholders to drive consistency, quality, and operational excellence across global content review and approval activities. Key Responsibilities: Medical & Scientific Review •       Conduct Medical and scientific review of promotional and non-promotional content, including Commercial, Medical Affairs, congress, digital, and field-facing materials, to ensure accuracy, balance, consistency, and alignment with approved data, product labeling, and scientific evidence in the literature. •       Evaluate scientific statements, references, data presentation, and clinical context for appropriateness and supportability. •       Provide clear, actionable, and scientifically grounded review feedback. •       Serve as the designated Medical reviewer within MLR and cMLR review processes for assigned therapeutic areas, brands, or content portfolios. Content Factory Scientific Partnership •       Partner with Content Factory teams and stakeholders to provide scientific guidance throughout content planning, development, and review activities. •       Advise on evidence requirements, scientific statements (Medical) and claims (commercial) substantiation, scientific communication objectives, and communication of clinical data. •       Support development of reusable and globally scalable content by promoting consistency in scientific communication and evidence utilization, aligned with the approved Scientific Communication Platforms and Lexicons for related assets. •       Identify and proactively address scientific-review risks to enhance content quality and review readiness. Cross-Functional MLR/cMLR Collaboration •  Participate in MLR/cMLR review discussions requiring scientific expertise and Medical judgment. •       Provide clear direction to project owners during the end-to-end lifecycle of the review, starting at the concept review stage until final approval for dissemination.