• NEW
  • 常勤
  • 東京都

【東京都品川区】外資系大手製薬メーカーMA

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（肥満症/MASH領域）

  • 300423897
  • 2026年04月07日更新
  • 当直なし
  • オンコールなし
勤務地 東京都品川区
給与（年収） 1000万円 応相談
募集科目 一般内科、循環器内科、内分泌内科、糖尿病内科、腎臓内科、その他、製薬会社
交通アクセス ***
医療機関区分 その他会社
病床数 ・・・
屋内の受動喫煙対策 敷地内禁煙

この求人に問合せる無料

この求人に問合せる無料

求人情報

勤務内容・条件

募集科目 一般内科、循環器内科、内分泌内科、糖尿病内科、腎臓内科、その他、製薬会社
勤務内容 その他
対象専門科目：内科、循環器内科、糖尿病内分泌科、腎臓内科

仕事内容：
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 ○○ make development/data building decision based on total picture (all projects/trials in the respects of resource/budget) in the TA.
・Strengthen ○○ 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.
Job Complexity
Work in a cross-functional team including MSL, CPL, PV (Pharmacovigilance), BDS (Biostatistics & Data Sciences), Marketing, Market Access in local and global team.
Interfaces
Integrated brand team, rapid response team, MST, MAST (Medical Affairs Subteam), Team Member Global Epidemiology, local R&D team members
週勤務日数 5.0日
勤務時間 (月～金) 09時00分 ～ 17時30分
週5日（月～金曜日）
9：00-17：30　（休憩時間60分）
フレックスタイム制（コアタイム無）
当直 なし

待遇・手当

給与（年俸） 1000万円 応相談
赴任手当 -
住宅手当 -
宿舎の提供 -
自動車通勤 -

福利厚生

休日 日曜日、祝日、土曜日
休暇 年末年始、その他休暇、初年度有給休暇
研究日 なし
社会保険 健康保険、雇用保険、労災保険、厚生年金
学会出席 -

その他

試用期間 あり（6カ月）同条件
備考 ・勤務地：東京都品川区
・年収1000万円～（目安）※経験・スキルによります。
・時間外労働：あり
・加入保険
　　社会保険：健康保険、厚生年金保険
　　労働保険：雇用保険、労働者災害補償保険

【必須条件】
・日本および海外の社内外のステークホルダーとの円滑なコミュニケーションおよび交渉能力（必須）。
・臨床または研究現場でのTA（テクニカルアシスタント）経験。特に肝臓関連疾患や、肥満・糖尿病などの代謝性疾患に関する経験があることが望ましい（強く推奨）。
・各疾患領域におけるキーオピニオンリーダー（KOL）や外部専門家との連携・マネジメント経験（推奨）。
・前臨床または臨床研究の構想立案、および科学論文の作成経験（推奨）。
・英語コミュニケーション能力（CEFR B2レベル以上が望ましい）

【歓迎スキル】
・医療製品の上市経験があれば尚可。
・臨床研究／臨床試験／臨床開発に関連する規制に関する知識があれば尚可。
・PMDAへの相談、新薬承認申請（NDA）の提出、および製品上市に関連する臨床開発および規制当局とのやり取りの経験があれば尚可。

この求人に問合せる無料

電話からのお問い合わせ

0120-337-613

電話をかける

受付時間：9:00〜18:00（平日）

関連する常勤求人

2026年04月08日更新

300423868

  • 当直なし
  • 週4以下
  • オンコールなし

【東京都足立区】内科系医師募集

勤務地
東京都足立区
給与
1200万円 ～ 1800万円 応相談
募集科目
内科全般（科目不問）、一般内科、呼吸器内科、消化器内科、循環器内科、内分泌内科、糖尿病内科、脳神経内科、血液内科、腎臓内科、老人内科、リウマチ内科、総合診療科
勤務内容
外来、病棟
★勤務内容は柔軟に相談可能です（病棟管理のみ希望など）

■病棟管理
25～30名程度（障碍者病棟）
障碍者病棟は重度の肢体不自由者、意識障害者、脊髄損傷の重度障害者、及び神経難病の方を対象にした病棟で、長期の入院を受け付けております。また、在宅療養で介護をしているご家族等の介護休暇（レスパイト）入院も実施しています。手技としては、挿管、CV挿入は一部対応をお願いしておりますが、難しい場合は他の常勤医師に相談可能です。人工呼吸器は25％程度の導入率となります。（技師在籍）また、８～9割はDNARを取得しており、夜間や休日に呼び出されることは基本ありません。

■外来　　
0～5/コマ　※1～2コマ
主な症例…一般内科（風邪、発熱など）
1日0名の場合もあるため待機業務のようなイメージです。

■往診
施設往診　週1コマ（60名くらい）
　※往診は院長が担当していますが、今後施設が増えた場合や不在時などは対応を相談させてもらう場合があります。

■救急　
救急搬入なし

■当直
なし（希望者は相談可能）

■オンコール
基本当直医が対応しますので、稀に電話相談は入る可能性はあります。ただし、基本出動頂くことはありません。

■早番・遅番
あり（なしの相談可）

・紙カルテ

2026年04月07日更新

300423904

  • 当直なし
  • オンコールなし

【東京都新宿区】外資系大手製薬メーカーMA

勤務地
東京都新宿区
給与
1000万円 応相談
募集科目
一般内科、小児科、その他（感染症内科）、製薬会社
勤務内容
その他
対象専門科目：内科、感染症内科、小児科

仕事内容：
About the job
As Medical Scientific Liaison (Vaccine) within our Vaccines Medical team, you'll be the vital connection between cutting-edge vaccine science and healthcare professionals across Japan, building trusted relationships and sharing scientific insights that help protect millions of lives. Ready to get started?

Join the team protecting half a billion lives every year with next-gen science, mRNA innovation, and AI-driven breakthroughs. In Vaccines, you'll help advance prevention on a global scale - and shape the future of immunization. As a field-based MSL, you'll serve as the extension of our medical function, developing enduring partnerships with key opinion leaders and healthcare institutions throughout Japan.

About ○○:
We're an R&D-driven, AI-powered biopharma company committed to improving people's lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people's lives.

Main responsibilities:
Build and maintain trusted scientific partnerships with healthcare professionals, key opinion leaders, and medical institutions across Japan through proactive field engagement
Deliver high-quality, balanced scientific information during one-to-one interactions and group settings, responding to unsolicited requests with accuracy and expertise
Organize and facilitate local scientific meetings including hospital staff meetings and webinars, aligned with stakeholder engagement and country medical plans
Generate valuable insights from field interactions and collaborate with internal teams to inform medical strategy and evidence-generation activities
Support investigator-initiated research submissions and manage local advisory boards in full compliance with regulatory requirements
Communicate the clinical value of vaccine products to healthcare decision-makers and contribute to population health outcomes
Travel extensively (80%) across Japan to engage with healthcare professionals and build meaningful scientific relationships

2026年04月07日更新

300423903

  • 当直なし
  • オンコールなし

【東京都港区】外資系大手製薬メーカーMA

勤務地
東京都港区
給与
1000万円 応相談
募集科目
眼科、その他、製薬会社
勤務内容
その他
対象専門科目：眼科

仕事内容：
Objectives:

Medical Science Liaisons (MSL) will ensure that proper relationships with both established and emerging external experts (EEs) in Ophthalmology and Eyecare disease treatment are developed and nurtured ,and that our scientific credibility is advanced as planned. This position is based in Tokyo and will report to the MSL Manager, Eyecare.

Key Responsibilities:

Develop and maintain key scientific knowledge for credible dissemination of Eyecare and Ophthalmology related scientific information to external experts and healthcare professionals.
Identify qualified external experts to engage with in collaborative efforts such as Advisory Board meetings, medical educational programs, congress symposia and potential research collaborations.
Conduct with high integrity infield activities as determined by the annual medical functional plan and properly document outcome of scientific engagements with targeted external experts.
Provide scientific support to and maintain relationships with targeted external experts in Eyecare area including key academic societies by delivering credible scientific presentations through individual or in group interactions.
Provide external ophthalmic surgical experts with scientific and technical support to ensure ophthalmology surgical devices are properly used in clinical settings.
Work with local Medical Information as appropriate to ensure responses to the unsolicited scientific requests including off-label information on ○○ medicines are accurate, up to date, reviewed and approved by local relevant internal and external procedures.
Act as the point of contact for potential investigators by facilitating the communication with Area/Global Medical team on investigator-initiated study (IIS) ideas related to ○○ products and/or pipeline assets.
Attend scientific meetings/conferences and develop summaries of key data presented to be shared with the Brand Team and other internal stakeholders.
Comply with all applicable local and international laws and regulations, guidelines, codes of conduct, ○○ standards, policies and procedures.
Work cross-functionally with commercial and other internal stakeholders as needed to achieve the Brand Team business objectives.
Attend all assigned training courses to acquire and update job related knowledge and skills.
Upon request, assist prescribers with requests for access to ○○ medicines on a named patient or compassionate use basis, subject to all applicable legal and regulatory requirements.

2026年04月07日更新

300423901

  • 当直なし
  • オンコールなし

【東京都港区】外資系大手製薬メーカーMA

勤務地
東京都港区
給与
1000万円 応相談
募集科目
形成外科、皮膚科、その他、製薬会社
勤務内容
その他
対象専門科目：皮膚科、形成外科

仕事内容：
Job SUMMARY:
The Medical Advisor role contributes to the development and implementation of medical strategy and plans at the country level, provides medical input into brand strategies and acts as “scientific responsible” providing medical guidance and governance for all relevant therapeutic areas ensuring support of the life cycle of all products and support of optimal access of new products.
Medical Advisor role plans and executes impactful external engagement to communicate science-related therapeutic areas & products within the responsibility with External Experts (EEs) at all relevant platforms.
Medical Advisor role collaborates with other functions e.g. regulatory, marketing, AMI, within the country to operate a successful○○ organization.
Medical Advisor role has oversight on medical information and product safety at the country level ensuring support as needed.

KEY DUTIES AND RESPONSIBILITIES:
% of Time or
Importance
Medical Plan Planning & Execution 45%
Responsible for preparation of country medical plans integrated in the brand plans and successful execution on timely manner within the defined budget.
Provide oversight of medical information activities in the country and support as required for the technical and scientific content of medical information enquiries.
Ensure all medical activities are compliant with appropriate SOP’s, Good Clinical Practice (GCP) ICH guidelines and all applicable local guidelines and legislations.

External Engagement 15%
Build long-term relationships with EEs discussing safety, efficacy, and data gaps
Identify new EEs for future engagement and involve EEs with○○ as advisors, investigators, trainers, speakers
Provide Speaker and Procedure Training Support
Gather Insights from EEs and share appropriately
Scientifically represent and support Medical Conferences and ○○ advisory boards and educational meetings
Attend key Conference and professional society engagements and generate conference and scientific session reports. Schedule meetings and Networking Events with EEs at Conference

Research support 5%
Identify and evaluate potential investigators for future ○○ studies
Conduct Study Awareness events as requested
May provide education or procedure training to study sites.
Disseminate clinical data to study investigators as requested by○○ Medical & Clinical teams
Provide scientific support at ○○ study sites and investigator meetings as requested
Facilitate EE/HCP understanding of○○ sponsored research and IIT strategies and processes
Provide support for local publications (e.g. local translation, proof reading, medical writing, literature search

Training and Education 10%
Develop and maintain expertise through review of Scientific Literature & training materials
Assist customization of scientific materials (slide decks, etc.)
Provide cross-functional scientific support within R&D
Upon request, provide scientific training and advice for commercial organization consistent with all relevant SOP & guidance documents

Brand Team Responsibilities 20%
Proactively contribute to creation and execution of brand plans and attend brand team meetings on regular basis.
Advise on promotional and any other relevant non-promotional materials and other relevant documents for medical accuracy and compliance with applicable guidelines and regulations.
Support regulatory and/or market access function from medical perspective to ensure optimal access of new assets to patients.
Support regulatory and/or market access functions from medical perspective for impactful life cycle management of Allergan Aesthetics products.
Support Allergan Medical Institute by providing medical input to local implementation of AMI strategies and tactics.
Provide medical input to consumer strategy for better patient outcomes
Provide medical input to digital strategy to ensure impactful digital engagement.

Professional and Personal Development: 5%
Assess performance levels, identify root causes and develop action plans for continuous improvement for areas of responsibility.
Implement the knowledge and skills gained in Allergan training programs to work practice and follow up.
Continue to develop and update product knowledge through reading textbooks, journal articles, and keep up to date with relevant scientific knowledge and participate and work in events including congress, symposia, field visits, training programs and be prepared to travel to the relevant location, where the function is required.
Take responsibilities in company projects and adapt him/herself to the changing or new work conditions and requirements.

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医師求人特集

  • 週4日の勤務可能の常勤 生活の質を重視する意思に評判！
  • 高額求人特集2,000万円以上可能！大幅な年収アップも可能
  • 管理職求人特集 キャリアアップ転職に最適
  • 医療機関求人特集 将来の開業に向けた支援がある
  • 福利厚生が充実している医療機関求人特集

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