募集要項
| 業務内容 |
Effective Management of a project including: Coordinate and manage project start-up, project maintenance, and project close-out activities; Maintain ongoing Sponsor contact for project-specific issues by serving as primary contact for Sponsor and all project team members; Track study status including patient status, Case Report Form status, safety issues, timelines, etc.; Serve as primary contact for protocol interpretations and logistical project-related issues (internal and external); Provide management oversight for Clinical Research Associates and Project Coordinators on project team; Interpret contract-related issues and coordinate company activities according to current scope; Develop study management tools, including communication plan, clinical monitoring plan, patient recruitment and retention plan; Communicate change in scope to Sponsor clinical team and Company Contract Manager. Provide input for following (when applicable): Study protocol Edit Check Specifications Data Analysis Plan Data clean-up results Analysis Final study report |
|---|---|
| 雇用形態 | 正社員 |
| 応募資格 |
Bachelor’s degree and 4 years related pharmaceutical industry experience (clinical monitoring or study management), or Master's degree/PhD with 2 years of related pharmaceutical industry experience (clinical monitoring or study management); Broad knowledge of medical terminology, clinical patient management, and clinical research methodology; Bilingual Japanese and English |
| 英語力 | ビジネスレベル |
| 年収 | 780万 〜 1800万円 |
| 給与詳細 | 年収：780万円～1800万円 |
| 勤務地 | 東京都 |
| 備考 |