常勤
東京都

【東京都北区】2026年6月開院・駅近クリニックの常勤医募集

高額給与　勤務日数相談OK！　土日祝休み＆当直・オンコールなしでプライベート充実◎

300417634
2025年07月28日更新

当直なし
週4以下
高額年俸
院長クラス
オンコールなし

勤務地	東京都北区
給与（年収）	1800万円～ 2000万円応相談
募集科目	皮膚科、その他
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
勤務内容	外来外来患者数（目安）：新規開院のため未定保険診療：美容診療の割合＝新規開院のため未定　　　　　※一部自由診療あり　レーザーや美容皮膚科診療(カウンセリング含む) 設　備：電子カルテ（CLIUS）体　制（目安）：常勤1名
週勤務日数	5.0日
勤務時間	(月～金) 09時00分～ 18時00分 ※週4日、3日検討可　 ※週3日の場合も社保加入可休憩時間：75分（概ね13:00-14:15）
当直	なし

待遇・手当

給与（年俸）	1800万円～ 2000万円応相談
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	日曜日、祝日、土曜日
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（6カ月）同条件
備考	給与：週5日年収1,800～2,000万円早番遅番・当直・オンコールなし時間外労働：有り（月数時間以内）残業代：10分ごとに支給

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

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受付時間：9:00〜18:00（平日）

関連する常勤求人

2026年06月12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.

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06月12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: 1200万円応相談
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06月12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: 1200万円応相談
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：
Objectives:
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06月12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: 1400万円応相談
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

・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.