- 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06月12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） | 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 |
| 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 |
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 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. |
| 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） | 1150万円 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 【応募条件】 Job Expertise Understandings of regulatory, clinical development, medical communication and compliance requirement in Medical Affairs Minimum Education/Degree Requirements A Master’s degree in life sciences. MD or PhD is preferred. Capabilities (Skills, Experience, Competencies) ・Good communication and negotiation skills for internal and external stakeholders in Japan and global (required). ・TA experience in clinical or research setting, ideally for a liver-related disease and metabolic diseases such as obesity and diabetes (strongly preferred). ・Experience in collaborating and managing key opinion leaders and external exports in respective disease area (preferred). ・Experience in conceptualization of pre-clinical or clinical research and in developing scientific manuscript (preferred). ・English communication skills (preferred CEFR B2 or above). ・Experience in medical product launch is plus. ・Knowledge about the regulations related to clinical research/clinical trial/clinical development is plus ・Experience in clinical development and regulatory interactions related to PMDA consultation and NDA filing and product launch are plus. Regarding publications ・Please submit list of key publications, if possible I relation to this field. |
