Principal Responsibilities Contribute to the TA strategy through researching the medical environment, identifying and building relationships with KEEs, and through the planning, preparation of advisory board meetings. Participate in program meetings to stay updated on the latest progress and provide expert opinions as needed to support team discussion and decision-making. Act as a point of contact for global clinical development expert Review and provide expert input on program related documents (e.g. protocol, IB) Review and/or provide expert input on documents for regulatory interactions (e.g. briefing document for PMDA, Orphan drug designation application) Review and provide expert input on relevant parts of filing documents (e.g. CTD, J-PI, RMP). Prepare responses to clinical part of PMDA inquiries in collaboration with JPTL and other JPT members. Contribute to discussion of PADG team in collaboration with JPTL and medical affairs. Review and expert input on publication strategy and contents/quality of publications. (In case of a Japan stand-alone study) create study documents (e.g. protocol concept sheet) Qualifications Minimum of eight (8) years of experience in drug development in pharmaceuticals, biopharmaceuticals, or biotechnology. Experience in Phases 1 to 3 as a clinical scientist. (Preferred) Experience working in a global pharmaceutical company Extensive experience as a clinical scientist including KEEs engagement, AdB meetings, preparation of clinical documents (e.g. protocol, IB), regulatory interactions, filing preparation and post-filing inquiry resolution. Knowledge of local regulations and guidances English skills that enables communication with global team. Education Life Science related bachelor’s degree Others Business Trip Available; Visit to mainly domestic medical institutions/doctors, domestic conferences, etc. Date Posted 13-7月-2026 Closing Date 11-7月-2027 Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact accommodations@Alexion.com. Alexion participates in E-Verify. For over three decades, patients and their caregivers have been at the center of everything we do. Every day, we are inspired to follow the science and think differently to create better outcomes for them and their families. Our mission is driven by understanding who they are as unique individuals, not solely defined by their diseases. We’re a leading rare disease company with a diversified projects. Our pioneering legacy in rare diseases is rooted in being the first to translate the complex biology of the complement system into transformative medicines over the past three decades. Today, we continue to push the boundaries of science and deepen our understanding of rare diseases with patient-centricity at the core. This knowledge allows us to innovate and evolve into new areas where needs are unmet and provide an opportunity to help people fully live their best lives.

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