主要职责:
• 在总体监督下'负责实施和监控临床研究'确保遵循公司标准和政府法规
• 为调查人员和研究参与者提供培训和相关信息
• 管理公司赞助的观察性研究'并为研究文件提交过程中涉及的监管事务提供支持
• 协助医疗顾问编写出版摘要和评估出版文献
• 根据需要为全球临床研发提供支持'以在研究方面达成一致
任职资格:
• 具有护理和药剂学专业学位'或科学/医学专业高等学位(医学博士,博士,药学博士)者优先
• 3-5 年制药/生物制药行业相关经验
根据当地法律和/或学历背景要求'可能会存在任职资格或岗位职责的差异。 请参阅适用于当地的工作描述文档。
About CSL Vifor
CSL Vifor aims to become the global leader in iron deficiency and nephrology.
The company is a partner of choice for pharmaceuticals and innovative patient-focused solutions across iron, dialysis, nephrology and rare conditions. CSL Vifor strives to help patients around the world with severe, chronic and rare diseases lead better, healthier lives. It specializes in strategic global partnering, in-licensing and developing, manufacturing and marketing pharmaceutical products for precision patient care.
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For more information, please visit viforpharma.com
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