常勤
東京都

【東京都港区】美容皮膚科クリニック

週4日2,000万円！働き方に応じた高収入が可能★

300422856
2026年02月24日更新

高額年俸

勤務地	東京都港区
給与（年収）	2000万円～ 3000万円応相談
募集科目	皮膚科、その他（美容皮膚科）
交通アクセス	最寄駅より徒歩２分
医療機関区分	クリニック
病床数	０床
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

求人情報

勤務内容・条件

募集科目	皮膚科、その他（美容皮膚科）
勤務内容	外来 ■カウンセリング：10名程度／日、しわ、たるみ、アンチエイジングの相談など ■注入：ボトックス、ヒアルロン酸、グロースファクター、リジュラン　など ■リフトアップ：糸 ■ブログ執筆（メニュー症例共有など）　※対応ノルマ無し、理事長からの指導予定　※SNSへの出演、お顔出しをお願いすることがございます。 ■ご自身の得意な対応・希望施術があればメニュー追加・指導も検討可能常勤体制：医師1名、看護師2名、受付1名主な疾患：美容皮膚科診療全般（強み：ほうれい線）カルテ　：電子カルテ
週勤務日数	4.0日～ 5.0日
勤務時間	(月～金) 10時00分～ 19時00分 (土曜日) 10時00分～ 19時00分月9休（週5勤務の場合）希望休は1か月前
当直	-

待遇・手当

給与（年俸）	2000万円～ 3000万円応相談
赴任手当	なし
住宅手当	なし
宿舎の提供	なし
自動車通勤	可

福利厚生

休日	その他
休暇	季節休暇、年末年始、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	なし

その他

試用期間	あり（条件確認中）同条件
備考	・勤務曜日相談・週4日以上時短相談等可能・週3日非常勤も相談可能・マイカー通勤可能（交通費として2万円まで支給）今後東海エリアや。中国エリアにも分院展開を予定のクリニックです。テナント探し等これからになりますので、新規開院を１から伴走頂ける可能性がございます。

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03月05日更新

300423243

当直なし
週4以下
オンコールなし

【東京都足立区】整形外科・脊椎外科

勤務地: 東京都足立区
給与: 1200万円～ 2000万円応相談
募集科目: 整形外科、その他（脊椎外科）
勤務内容: 外来、病棟、救急、手術
■外来診療：週2コマ程度（10～15名/コマ）

■病棟管理：一般・回リハ15～20名程度
病棟は主治医制ですが、当直帯は当直医が対応しますので呼び出されることは基本ありません。（電話相談のみ）

■救急対応：夜間含め0～2台/日
救外のコマを用意しているわけではなく、空いている常勤医師に対応頂くことになります。

■手術　　：1～4件/日（手術室は2室）
脊椎の症例が主となりますが、脊椎以外の手術もございますのでご専門が脊椎である必要がございません。

＜主な症例＞
脊椎疾患・外傷・関節疾患・変性疾患・リウマチ・骨粗鬆症・炎症性・過使用疾患・手の外科など

腰痛、坐骨神経痛、骨粗鬆症性脊椎骨折、頸椎椎間板ヘルニアなどに対し早期の社会復帰を実現するための最新の低侵襲手術の実施と研究を行っております。また、最近では内視鏡下腰椎椎間板ヘルニア切除術、骨粗鬆症性椎体骨折に対する椎体形成術、脊椎後弯症に対する矯正手術なども積極的に行っています。

2026年02月16日更新

300420689

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: 皮膚科、製薬会社
勤務内容: その他
対象専門科目：皮膚科

仕事内容：
Based on the Brand/Functional plan, develop and execute MSL Action Plan through scientific interaction
and connect to evidence generation and collectively, as member of GMA, work to make a remarkable impact
on patient care
Major Responsibilities:
1.KEE management
・Cultivate and develop scientific engagement with Medical Target KEEs
・Understanding the needs of developing strategic KEE interaction planning,
develop the strategic interaction plan appropriately
・Cultivate and maintain relationships with KEEs prior to product launch　through Multi-channel communication plan with KEEs
・Provide scientific information and have a discussion with EELs
・Provide accurate TA knowledge and scientific message to KEEs (non-product)
・Gain DPOs through scientific discussions
2.Coordinate Investigator Initiated Study (IIS) following new SOP (Contract-Based IIS)
・Get information of IIS plan with products and may proceed further process
with limited support
・Understanding the IIS process,
・Take a role of SME in proceeding the IIS process
・Support other departments in scientific point of view
・Provide scientific information
3.Active participation and effective communication for product maximization cross functionally
・Understand Brand Plan and Medical Plan for execution in the field
・Provide feedback from the field after implementation of the functional plan
・Identify appropriate KEEs for tactical action in Medical plan by understanding the target KEE's profile,
treatment policy and/or his/her point of view
4.One R&D collaboration (as needed)
・Understand the local action plan and its objectives to support clinical development
・Collaborate with Clinical Development in-field team to accelerate enrollment through scientific interaction
5.Team Management
・By understanding TA/ Team policy, contribute to the team management incollaboration with MSL Manager
・Support peer MSLs who have relatively less experience
6.iFTE playbook understanding & execution
・Understand the Medical and other key stakeholders' actions including Commercial in iFTE playbook
and execute accordingly
・Collaborate in-field as one team and support other team members in Medical

2026年02月16日更新

300422295

当直なし
オンコールなし

【東京・大阪・鹿児島】外資系CRO 臨床開発

勤務地: 東京都中央区、大阪市北区、鹿児島市※在宅勤務を想定
給与: 1000万円応相談
募集科目: 一般内科、脳神経内科、その他、製薬会社
勤務内容: その他
対象専門科目：神経内科、腫瘍内科、一般内科

仕事内容：
■Responsibilities: Project Related Medical/Safety Management:
◇Minimize potential risk to ○○ and clients by managing medical aspects of contracted tasks. This includes, but is not limited to, medical monitoring of all safety variables (AE, laboratory abnormalities, changes in patient medical status as well as inclusion/exclusion criteria, evaluation prescribed concomitant medication for protocol restrictions and unblinding requests). Scope of work also includes discussion internally with medical monitors in Japan, APAC and global and project team colleagues internally, as well as with principal investigators and clients of all medical issues during the course of a study by proper medical judgment, interpretation and decision.
◇Medical review of serious adverse events: Ensure tasks delegated to medical monitors are properly executed. Adhere to applicable regulations and ICH guidance regarding clinical trials, regulatory documents, and safety issues. Adhere to client SOPs/directives and project specific WPDs for assigned projects. Adhere to ○○’s corporate policies and SOPs/WPDs.
◇Present ○○ standard medical processes to clients at business development meetings, investigator meetings, and communicate with various medical communities to explore and expand ○○ business.
◇Provide medical consultation to team members and help manage protocol related medical questions. Communicate clearly with project team members and clients, maintaining open communication to ensure all procedures are followed appropriately. Provide therapeutic training and protocol training on assigned studies, as requested.
◇Perform listing reviews as specified in the client contract and data validation manual, including review of coding listings and/or full safety listings as well as use of Patient Profiles and other tools to assess for potential safety signal. This position will be assigned to APAC components of global or regional studies. Including but not limited to global/regional studies with Japan component.
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2026年02月16日更新

300422296

当直なし
オンコールなし

【東京都品川区】外資系大手製薬メーカーMA

勤務地: 東京都品川区
給与: 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
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 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
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・Responsible for making Japanese clinical development plan recognized by global Medicine as well aligned with global development strategy in the respective therapeutic area.
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・Gain insight from external expert with MSL (Medical Science Liaison) and propose medical strategy.

Regulatory and / or Organizational Requirements
Contribute to Strategy and Activity Review Committee meetings. Ensure ethics and compliance. Ensure re-examination by reviewing documents and process. Plan strategically to allow for effective, safe & medically sound global preparation of drug commercialization efforts. Provide input and medical review of all internal and external documentation prepared by Marketing and Public Relations. Define trials needed to answer relevant questions regarding our products and their related development projects to meet regulatory and payer requirements and our commercial needs build upon from the trial’s concepts developed by the Medical subteam and local project team for registration. Provide medical input into epidemiology studies. Ensure communication with CPL (Clinical Project Leader). Support obtaining preferable pricing.

Job Complexity
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