常勤
東京都

【東京都豊島区】クリニック／糖尿病内科

週2.5日勤務（社会保険付帯あり）／年収1,050万円～／駅チカ

300422599
2026年02月17日更新

外来のみ
週4以下

勤務地	東京都豊島区
給与（年収）	1050万円～ 1200万円応相談
募集科目	糖尿病内科
交通アクセス	最寄駅より徒歩1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	糖尿病内科
勤務内容	外来、健診 ■糖尿病外来、一般内科外来、健康診断など ※一般内科全般、生活習慣病外来、急性胃腸炎の様な一般的な消化器疾患など ※特定健診、企業健診、雇用前健診などを随時実施しております。・外来数30名程度/コマ・消化器内科医と2〜3診体制・予約制・電子カルテ（BML）
週勤務日数	3.0日
勤務時間	(月～金) 09時00分～ 18時30分 (土曜日) 09時00分～ 13時30分・週2.5日勤務　※弊社システムの都合で週3日で登録しています・勤務曜日：水曜、金曜、土曜　※曜日固定
当直	-

待遇・手当

給与（年俸）	1050万円～ 1200万円応相談
赴任手当	-
住宅手当	-
宿舎の提供	-
自動車通勤	不可

福利厚生

休日	日曜日、祝日、土曜日(午後)、その他
休暇	初年度有給休暇
研究日	なし
社会保険	労災保険
学会出席	-

その他

試用期間	なし
備考	消化器専門のクリニックでの糖尿病外来の求人です。糖尿病専門医をお持ちの先生歓迎。・予約制のため、残業はほぼありません。・各種保険：労災保険

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

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: 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 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

2026年04月07日更新

300423896

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 clinical development and late stages of commercialization.
Accountabilities
・Strengthen value of our products by providing medical/scientific robust guidance in the responsible therapeutic area 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 our company make development/data building decision based on total picture (all projects/trials in the respects of resource/budget) in the therapeutic area.
・Prepare Integrated Customer Plan (ICP) 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, external collaborative research 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.
Regulatory and / or Organizational Requirements
Contribute to strategy and activity review meetings. Ensure ethics and compliance. 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. Ensure communication with CPL (Clinical Project Leader). Support obtaining preferable pricing.
Job Complexity
・Works in a cross-functional team including MSL, CPL, RA (Regulatory Affairs), PSPV (Patient Safety & Pharmacovigilance), BDS (Biostatistics & Data Sciences), Marketing, and Market Access. Requires driving cross-functional projects.
・Plays a key role in planning and leading medical strategy initiatives in collaboration with internal and external stakeholders.
Interfaces
Integrated brand team, Local/Global R&D team members, Medical Affairs subteam, Team member global epidemiology, etc.

2026年04月07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
・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.

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
・Works in a cross-functional team including MSL, CPL, RA (Regulatory Affairs), PSPV (Patient Safety & Pharmacovigilance), BDS (Biostatistics & Data Sciences), Marketing, and Market Access
・Requires driving cross-functional projects. People management responsibilities may be assigned depending on the candidate’s career background and organizational needs.
・Plays a key role in planning and leading medical education initiatives in collaboration with internal and external stakeholders.