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| Hiring Company | 外資スペシャリティファーマ |
| Location | Tokyo - 23 Wards |
| Job Type | Permanent Full-time |
| Salary | 13 million yen ~ 16 million yen |
【求人No NJB2320559】
治療領域戦略の策定に向け、医療環境の調査や主要意見者との関係構築、アドバイザリーボードの企画・準備を行います。
プログラム会議に参加し進捗を把握、専門的意見を提供してチームの意思決定を支援。グローバル臨床開発専門家との連絡役を担い、関連文書や規制対応資料のレビュー・意見提供を実施。申請書類の臨床部分も担当し、規制当局からの照会対応を準備。
| Minimum Experience Level | No experience |
| Career Level | Mid Career |
| Minimum English Level | Business Level |
| Minimum Japanese Level | Native |
| Minimum Education Level | Bachelor's Degree |
| Visa Status | Permission to work in Japan required |
Qualifications
Minimum of eight (8) years of experience in drug development in pharmaceuticals biopharmaceuticals or biotechnology.
Experience in Phases 1 to 3 as a clinical scientist.
(Preferred) Experience working in a global pharmaceutical company
Extensive experience as a clinical scientist including KEEs engagement AdB meetings preparation of clinical documents (e.g. protocol IB) regulatory interactions filing preparation and post filing inquiry resolution.
Knowledge of local regulations and guidances
English skills that enables communication with global team.
Education
Life Science related bachelor’s degree
Others
Business Trip Available; Visit to mainly domestic medical institutions/doctors domestic conferences etc.
| Job Type | Permanent Full-time |
| Salary | 13 million yen ~ 16 million yen |
| Work Hours | 09:00 ~ 17:15 |
| Holidays | 【有給休暇】有給休暇は入社時から付与されます 入社初年度は入社月により4日~16日を付与。 翌年1月1日から年20日付与。有給… |
| Industry | Pharmaceutical |
| Company Type | International Company |