**Organization:** Transformation office, New Product Planning **Report to:** Associate Director, New Product Planning **Main purpose of job:** + Drive commercial assessment of the early asset pipelines especially from scientific perspectives until the BT (Brand Team) is established and ensure a smooth transition of information and assessment outcomes from NPP to the BT + Aim to maximize the potential of new assets by assessing the candidate assets, aligning with corporate strategy, and addressing unmet medical needs in Japan from early development phase + Evaluate assets from a medical perspective and supports decision-making in the early stages on both clinical development strategy and future commercial strategy perspectives **Responsibilities;** **Analyze disease landscape and identify unmet local medical needs in Japan** + Conduct literature reviews, guideline analyses, and secondary research using available databases (e.g., epidemiology reports, treatment pattern data) + Perform quantitative market analysis utilizing syndicated data sources to estimate patient populations, treatment flows, and market dynamics + Summarize and systematize findings into structured disease landscape reports that highlight gaps in current medical practice + Consolidate insights from internal knowledge-sharing sessions (e.g., feedback from Medical Affairs colleagues who engage with KOLs) to strengthen internal understanding of unmet needs **Evaluate the medical validity of the Target Product Profile (TPP)** + Review the TPPs prepared by Global teams against Japan-specific treatment standards and regulatory requirements + Map out discrepancies between the global TPP and local medical practice, including endpoints, dosing regimens, or comparator relevance + Provide medical assessments and summarize the alignment/misalignment with Japanese clinical realities (if required) **Assess medical feasibility of development assets** + Prepare comparative analyses of development assets against current standard of care and competing pipeline products + Develop internal briefing reports assessing potential clinical impact, positioning, and value of the asset in the Japanese treatment landscape + Conduct scenario modeling to evaluate how the asset may shift treatment paradigms or address patient subgroups with unmet needs + Collaborate with internal experts (R&D, regulatory, Medical Affairs colleagues) to validate assessments and align perspectives **Develop medical evidence generation plans (internally driven)** + Identify data gaps relevant to the Japanese market through desk-based gap analysis of available clinical and real-world evidence + Collaborate with Medical Affairs colleagues to refine study concepts and prioritize evidence generation opportunities **NOTE: This position DOES NOT belong to the Medical Affairs Department** **Basic Qualifications** + 5+ years of work experience in the pharmaceutical industry and had experience collaborating with commercial functions + Advanced degree in medicine, pharmacy, or life sciences (Master's or PhD preferred) + Knowledge of medical evidence evaluation and generation + Experience collaborating with cross-functional teams in local (Japan) + Experience collaborating with global teams/colleagues **Preferred Qualifications** + Experience in early-stage clinical development and strategic planning + Strong understanding of disease mechanisms and treatment paradigms + Both Japanese and English (business level); fluency in speaking, writing and reading **Work Style:** + Remote work is supported. However, applicants must be able to commute to the office flexibly when needed. Office attendance is expected on an occasional basis, typically around twice per month.