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| Hiring Company | 大手外資製薬メーカー |
| Location | Tokyo - 23 Wards |
| Job Type | Permanent Full-time |
| Salary | 8 million yen ~ 10 million yen |
【求人No NJB2343596】
グローバル臨床試験の実行を担う中央チームの一員として、複数のフェーズ0~4試験の計画・実行・管理を支援します。
プロジェクトマネージャーの指導のもと、品質・効率・スケジュール・予算を遵守し、戦略目標達成に貢献。ベンダー管理、被験者募集戦略の立案・実行、会議運営、リスク管理、関連文書の作成・管理、システム運用支援など多岐にわたる業務を担当。検査対応や教育支援、プロセス改善にも積極的に関与します。
| 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
・ Bachelor’s Degree or OUS equivalent required
・ Must have at least 2 years of pharma/device or clinical research related experience with a moderate level of core and technical competencies
・ Competent in application of standard quality procedures (SOP ICH/GCP Global Regulations)
・ Analytical and critical thinking skills to evaluate complex issues from multiple perspectives and contribute to strategy and smart decision making to support acceleration of study timelines and enable a well run study
・ Excellent organizational and time management skills strong attention to detail.
・ Strong interpersonal skills with ability to communicate effectively in a clear and persuasive manner; proficient in business/technical English language (oral and written)
・ Proactive collaborative mindset
・ Ability to work independently in a fast paced global team environment
・ Preferred: Experience with 1 or more clinical trial systems (e.g. EDC IRT CTMS eTMF); experience in 1 or more parts of a clinical trial
| Job Type | Permanent Full-time |
| Salary | 8 million yen ~ 10 million yen |
| Work Hours | 08:45 ~ 17:30 |
| Holidays | 【有給休暇】初年度 10日 1か月目から付与 ※初年度有給休暇は入社日によって付与日数が異なります 【休日】完全週休二日制 土… |
| Industry | Pharmaceutical |
| Company Type | International Company |