常勤
東京都

【東京都足立区】脳神経外科（脊椎脊髄外科）　指導医・専門医歓迎

外来・病棟・オペ　週4～5日　高年収可能　当直・オンコールなし

300420477
2025年12月03日更新

当直なし
週4以下
高額年俸
オンコールなし

勤務地	東京都足立区
給与（年収）	1800万円～ 2200万円応相談
募集科目	脳神経外科、その他（脊椎脊髄外科）
交通アクセス	東武スカイツリーライン最寄駅より送迎バスあり
医療機関区分	一般
病床数	20床以上100床未満
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	脳神経外科、その他（脊椎脊髄外科）
勤務内容	外来、病棟、手術・外来／1コマ20～25名程度を想定・病棟管理／10～15名程度を想定・オペ／病院全体で1日6～7例程度を想定（オペ室3室）・当直なし（当直希望の場合は別途手当あり）・オンコールなし
週勤務日数	4.0日～ 5.0日
勤務時間	(月～金) 09時00分～ 18時00分 (土曜日) 09時00分～ 18時00分
当直	なし

待遇・手当

給与（年俸）	1800万円～ 2200万円応相談
赴任手当	応相談
住宅手当	応相談
宿舎の提供	-
自動車通勤	-

福利厚生

休日	日曜日、祝日
休暇	初年度有給休暇
研究日	あり
社会保険	健康保険、雇用保険、労災保険、厚生年金
学会出席	あり年1回まで(発表の場合は別途相談可)

その他

試用期間	なし
備考	2023年オープンの綺麗な病院です。 100床以下・救急指定はありません。当直医で夜間対応は行いますのでオンコールもありません。 ON/OFFメリハリのついた勤務が可能です！【給与】週5日の場合専門医　1,800万円～　当直料別途　指導医　2,200万円～　当直料別途

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

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.

2026年06月12日更新

300423897

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: 1150万円応相談
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 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 NBI make development/data building decision based on total picture (all projects/trials in the respects of resource/budget) in the TA.

・Strengthen NBI 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.