医師転職・バイトは民間医局

東京都・内科・循環器内科の常勤医師求人（26-JQ314780）

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    • 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08月04日   案件番号 : 26-JQ314780

    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/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
    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 to make development/data building decision based on total picture (all projects/trials in the respects of resource/budget) in the TA.
    ・Strengthen our products’ profile by providing medical/scientific robust guidance in the responsible TA through the total process of the clinical development phases, in collaboration with the 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 the 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
    900万円～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、積立休暇、慶弔休暇、リフレッシュ休暇、ボランティア休暇、看護等休暇等、初年度入社時有給休暇：10日、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
    Education/Experience Required:

    Undergraduate degree in medical science or pharmacology is a MUST and advanced degree (e.g.: MD, PharmD, PhD or MSc) in relevant scientific discipline is preferred.
    Solid knowledge of the pharmaceutical environment and the role of Medical Affairs to advance the medical and scientific objectives.
    Professional experience in neuroscience field as MSL, CRA or in a similar field-based R&D role of at least 3 years is a MUST.
    Key in-Field Team (IFT) Competencies:

    Ability to comprehensively learn new subject areas and environments and keen interest in developing and maintaining expert knowledge for assigned therapeutic area/product and medical research in general.
    Ability to coordinate scientific/medical engagement efforts across stakeholders within a single account in order to develop interaction plans that are in-line with the Scientific Interaction Plan (SIP) to achieve medical objectives.
    Ability to understand the unmet needs of key stakeholders, make decisions that have an impact and execute the integration and assimilation of that information into the In-field Team (IFT) engagement approach.
    Effectively communicate, collaborate and incorporate the views of other in-field team members to optimize business objectives.
    Collaborate effectively with Clinical Development in-field teams for acceleration of patient enrollment in clinical studies designated as “enterprise critical” through scientific engagement with Principal Investigators.


    Essential Skills & Abilities:

    Proficient with Microsoft Office Suite (Outlook, PowerPoint, Excel, Word, etc.)
    Must be at ease with technology (the use of various tools/systems to perform day-to-day tasks).
    Excellent written and spoken communication as well as presentation skills in Japanese, with a demonstrated ability to develop and maintain strong collaborative relationships with thought leaders, physicians and other healthcare decision makers.
    High proficiency in English reading, writing and speaking skills highly preferred (Versant Score: >43)
    Drive results through high customer orientated mindset.
    This function is typically field based with up to 20% of an individual’s working time spent in the office and remaining 80% in the field.

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