東京都・内科・循環器内科の常勤医師求人(26-JQ310984)

    • 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-JQ310984

    担当エージェントより

    募集形態:メディカルアフェアーズグループマネージャーorメディカルアドバイザー/グループマネージャーorノンラインマネージャー /医薬開発本部クリニカルディベロップメント・メディカルアフェアーズ心・腎・代謝領域
    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 contribute to execute CDMA (Clinical Development & Medical Affairs) activities in Japan according to TA (Therapeutic Area) strategy between start of preclinical development and late stages of commercialization.

    Accountabilities
    ・Strengthen the profile of our products by providing medical/scientific robust guidance in the responsible therapeutic area through the total process of the clinical development phases, in collaboration with Global and other departments.
    ・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 global Medicine as well aligned with global development strategy in the respective therapeutic area.
    ・Support our company make development/data building decision based on total picture (all projects/trials in the respects of resource/budget) in the therapeutic area.
    ・Contribution to CDPs (Clinical Data Packages) after proof of concept and late stages of commercialization.
    ・Prepare Integrated Customer Plan to address Japan specific needs, together with Marketing and Market Access & aligned with global IAP (Integrated Asset Plan).
    ・Build new scientific evidence by collaboration with external experts through clinical/pre-clinical researches, investigator initiated studies and RWE (Real World Evidence) studies.
    ・Contribution to benefit/risk evaluations of products.
    ・Gain insight from external expert with MSL (Medical Science Liaison) and propose medical strategy.
    給与
    ~1,400万円(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
    Minimum Education/Degree Requirements
    Master's degree in life sciences. MD or PhD is preferred.

    Required Capabilities (Skills, Experience, Competencies)
    ・TA experience in clinical or research setting, ideally for nephrology, cardiology and endocrinology
    ・Experience in clinical development and regulatory interactions related to PMDA consultation and NDA filing and product launch are preferred
    ・Capability to conceptualize research projects, conduct basic and/or clinical research independently, and write scientific papers
    ・Experience collaborating with and managing key opinion leaders and external experts in relevant disease areas
    ・Strong negotiation and communication skills for both internal and external stakeholders, in Japan and globally
    ・Excellent project management and cross-functional collaboration skills, with the ability to work in global matrix teams
    ・Experience designing, developing, and delivering medical education programs using in-house media or third-party platforms
    ・Experience leading team projects (evidence generation, new drug launch/approval, collaboration with external stakeholders) ; people management experience is preferred.
    ・English proficiency (at least TOEIC >800)
    ・Knowledge of regulations related to clinical research, clinical trials, and clinical development

    Regarding publications
    ・Please submit publication's title and Author.

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