|部署・役職名||Sr Medical Advisor R＆D Oncology|
Purposes of the job are：
・Responsible for leading the relevant Japan development team （called ‘Japan Evidence
Generation Team’, JEGT）, and developing an integrated Japan development plan
incorporating local current medical/clinical insights into specific molecules in accordance with global development strategy.
・Contribute medical/clinical expertise to advancing our pipeline
・As the lead of the JEGT, appropriately share Global EGT strategies to the JEGT members,
indicate strategic direction of JEGT in accordance with global strategy and ensure that Japan product strategies are based on multifaceted considerations aiming to maximize values for patients and us.
・As the lead of JEGT, encourage active and efficient work styles in accordance with the Team Charter and build an environment where each member can utilize their full potential
・Provide deep local medical/clinical and scientific （as applicable） insights to local and global product teams
・Partner with Regulatory Affairs to facilitate local registration by providing medical/scientific leadership and input into key regulatory deliverables, i.e. CTD, Regulatory responses, etc.
・Partner with Local Development Operations to ensure timely delivery of high quality clinical data.
・Support the Local Medical Affairs in capturing and translating local data gaps into actionable evidence generation plans （EGPs）, in alignment with global product strategy and global EGP.
・As the clinical expert on the product, communicate the total evidence and biologic insights with internal stakeholders to align and inform their strategies, and with external stakeholders （KOLs / investigators, regulators, and payers） to shape the practice of medicine
・Medical Degree and/or PhD and/or equivalent experiences
・Deep scientific expertise in relevant therapeutic area
・Minimum of 5 years in pharmaceutical industry, or proven industry collaboration in academia
・Experience in leading Clinical Development and NDA filing
・Experience with clinical study management and conduct
・Knowledge of commercialization and business practices
・Deep understanding of pharmaceutical product development, product lifecycle and
commercialization process with advanced understanding of other functions; including but not limited to Clinical Operations, Commercial, Regulatory, and Medical Affairs, Value Access and Policy
・Oncology/Haematology area knowledge and demonstrated ability to rapidly develop deep understanding of new therapeutic areas
・Strong customer orientation; science based and marketing minded
・Existing network of OL contacts in therapeutic area
・Finance and budgeting experience
・Operational excellence: self management skills, planning, prioritization, objective setting, meeting management, plan execution
・Interpersonal skills: ability to engage with key stakeholders at a professional and clinical level