東京都・内科・循環器内科の常勤医師求人(26-JQ312092)

    • 常勤
    • 企業
    • 土・日・祝休み可

    大手外資系製薬会社での就業です

    掲載更新日 : 2026年06月17日   案件番号 : 26-JQ312092

    担当エージェントより

    募集形態:メディカルアドバイザー/ノンラインマネージャー or スタッフ/医薬開発本部クリニカルデベロップメント・メディカルアフェアーズ心・腎・代謝領域メディシン第3部(肥満症/MASH領域)
    対象専門科目:内科、循環器内科、糖尿病内分泌科、腎臓内科
    勤務地:東京都
    勤務地
    東京都
    路線
    科目
    内科・循環器内科
    勤務内容
    メディカルドクター
    勤務内容詳細
    Basic purpose of the job
    To plan and execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy. Confirmed target indication: Obesity disease, MASH (Metabolic dysfunction associated steatohepatitis).

    Accountabilities
    ・Gain insight from external expert (EE) with MSL (Medical Science Liaison) and propose medical activity based on identified medical gap.
    ・Build new scientific evidence by collaboration with external experts through clinical/pre-clinical researches, investigator initiated studies and RWE (Real World Evidence) studies including PMS.
    ・Prepare Integrated Asset Plan (IAP) & Detailed Annual Communication Plan to address Japan specific needs, together with Marketing and Market Access & aligned with global IAP.
    ・Support NBI make development/data building decision based on total picture (all projects/trials in the respects of resource/budget) in the TA.
    ・Strengthen NBI products’ profile by providing medical/scientific robust guidance in the responsible TA through the total process of the clinical development phases, in collaboration with BI corporate and other department.
    ・Ensure and support Japanese submission and registrations in the respective products collaborating with regulatory/ clinical development team. (Support the clinical part until approval, such as preparation of responses to PMDA queries.)
    ・Responsible for making Japanese clinical development plan recognized by BI global medicine as well aligned with global development strategy in the respective TA
    ・Contribution to CDPs (Clinical Data Packages) after proof of concept and late stages of commercialization with medical perspective.
    ・Contribution to benefit/risk evaluations of products.
    ・To understand and comply with regulations and industry rules (promotional codes, fair competition rules, privacy, data collection/storage, etc.) as well as related SOP.
    給与
    ~1,150万円(スキル・経験による)
    勤務日数
    週5日(月~金曜日)
    日程/時間
    8:45~17:20 配属先部門によりシフト勤務・フレックスタイム制の適用有り ※休憩時間:45分
    オンコール
    休暇・研究日
    年間休日131日(2025年度実績)、完全週休2日制(土日祝日)、年末年始、ゴールデンウイーク、お盆期間を中心に年3回程度の長期休日あり、初年度入社時有給休暇:10日 ※初年度は4/1入社時に10日分の年次有給休暇を付与します。入社翌年以降は、毎年1/1付けで新たに年次有給休暇(2年目14日)を付与します。半休および年次有給休暇の1時間単位の使用あり
    勤務開始時期
    応相談
    医療機関情報
    医療機関形態:企業

    屋内の受動喫煙対策:あり(禁煙)
    備考
    Job Expertise
    Understandings of regulatory, clinical development, medical communication and compliance requirement in Medical Affairs
    Minimum Education/Degree Requirements
    A Master’s degree in life sciences. MD or PhD is preferred.

    Capabilities (Skills, Experience, Competencies)
    ・Good communication and negotiation skills for internal and external stakeholders in Japan and global (required).
    ・TA experience in clinical or research setting, ideally for a liver-related disease and metabolic diseases such as obesity and diabetes (strongly preferred).
    ・Experience in collaborating and managing key opinion leaders and external exports in respective disease area (preferred).
    ・Experience in conceptualization of pre-clinical or clinical research and in developing scientific manuscript (preferred).
    ・English communication skills (preferred CEFR B2 or above).
    ・Experience in medical product launch is plus.
    ・Knowledge about the regulations related to clinical research/clinical trial/clinical development is plus
    ・Experience in clinical development and regulatory interactions related to PMDA consultation and NDA filing and product launch are plus.

    Regarding publications
    ・Please submit list of key publications, if possible I relation to this field.

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