東京都千代田区・内科の常勤医師求人(26-JQ310973)

    • 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02月24日   案件番号 : 26-JQ310973

    担当エージェントより

    募集形態:Clinical Leader
    対象専門科目:内科 ※抗がん剤治療経験
    勤務地:東京都千代田区、大阪府大阪市
    勤務地
    東京都千代田区
    路線
    科目
    内科
    勤務内容
    メディカルドクター
    勤務内容詳細
    Leads the Clinical Team, a cross functional, team of internal experts, through clinical phase I – III trials, and global product registration. Deal with relative complex projects (e.g. co-development with another company). Sets project-related objectives with team members. Requests clinical team members and clarifies resource availability with functional heads
    Act as a member of the J-Project Team representing Clinical Development (CLD) and member of the Launch team, representing CLD. Build consensus by complying input from multiple functions
    In consultation with relevant key disciplines, prepares the Clinical Development Plan (CDP). Responsible for planning and managing the clinical timelines, against the approved CDP. Provides domestic study concepts to ensure compliance with global strategy. Proactively initiates corrective action as needed
    Responsible for the ongoing risk-benefit assessment of a compound until approval in Japan. Analyses incoming clinical data, relevant medical and scientific information and initiates actions or decisions as appropriate
    In consultation with the Head of CLD and Global Clinical leader, responsible for assessments and communication of medical project and study strategy, study results and clinical project results to internal and external bodies (e.g. regulatory authorities)
    Responsible for defining the strategic approach and managing preparation of medical sections of key Regulatory documents (J-CTD Module 2s). Consults with Global clinical leader, Clinical Science, Clinical Statistics, Regulatory, PHV. Compiles and maintains Translated Investigators’ Brochures (IB)
    Provides medical expertise to Marketing (for marketed products and for development projects) and defines together with the Medical Affairs (MA) the publication strategy. Ensures consistency of publications with clinical data and publication strategy.
    →備考に続く
    給与
    年収1,000万円~(目安の金額になります)
    ※経験・スキルによります。
    勤務日数
    週5日(月~金曜日)
    日程/時間
    9:00-17:30 フレックスタイム制 ※休憩時間:60分
    オンコール
    休暇・研究日
    完全週休2日(土・日)、祝日、年間有給休暇10日~20日(下限日数は、入社直後)、GW休暇、年末年始休暇【※年間休日日数125日】
    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
    Contributes to Opinion Leader development and publications strategy with implementation detail. Establishes and maintains appropriate external scientific advisory boards and assists in advocacy development. Provides medical assessment of in- and out- licensing opportunities of development projects
    Conducting Clinical Development tasks independently while seeking advice on exceptional or complex topics from senior clinical leaders and/or managers


    【必須条件】
    ・医師免許(抗がん剤治療経験)
    ・医薬品開発(プロトコル作成から医療レビュー報告書まで)の実務経験を有すること
    ・ビジネスレベルの英語力

    【歓迎スキル】
    ・PhD保有

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