Medical Advisor
募集要項
| 年収 | 800万～1300万 |
|---|---|
| 雇用形態 | 正社員 |
| 職種 | 医師、歯科医師、獣医 |
| 仕事内容 | 画像診断装置に強みのある会社として、造影剤を中心に、医療従事者に対する医薬品や機器の情報提供、当社と製薬企業との共同研究におけるサポート、PMS（Post Marketing Surveillance）のマネジメント、医薬品副作用に関する情報管理などを行っていただきます。 This role supports planning and coordinating activities for the conduct of clinical trials, including all operational aspects of a clinical project. This roles supports the project team to achieve quality results in a cost－effective timely manner and execution of assigned clinical trials from protocol concept through to clinical study report, in compliance with international GCP guidelines/regulations and company policies and procedures. Duties include: 1. Management of pharmacovigilance and postmarketing surveillance study to ensure that the management system is compliant with applicable regulations, standards and/or regional requirements. 2. Key role in presenting clinical evidence to regional and national meetings of key referral groups 3. Support investigator sponsored studies, opinion leader relations and giving product trainings. 4. Pr |
| 求める人材 | 【求める条件】 1. Medical doctor, pharmacist or related Life Sciences diploma 2. Three or more years of experience of project management or clinical operations of pharmaceutical clinical trials including postmarketing studies 3. Excellent presentation skills 4. Excellent oral and written Japanese and fluent English communication skills 5. Ability to travel 30－40％ of time 【歓迎条件】 1. Self－motivated with a proven ability of working to deadlines 2. Ability to work effectively in cross functional and cross border teams 3. Experience in any of Nuclear Medicine, Neurology, Radiology preferred 4. Good commercial acumen and experience in a commercial environment |
会社情報
| 会社名 | 会社名は非公開です |
|---|---|
| 業種 | 半導体・電子・電気機器 |
| 資本金 | - |
| 従業員数 | - |
