职位描述:

1.协助PM管理和解决试验相关的遗传办申报工作；

2.帮助PM与遗传办相关人员保持良好和有效的沟通；

3.负责遗传办相关文件申请，递交流程。

4.协调临床部行政事务的工作；

5.协助临床注册相关工作；

6.协助整理临床试验文档和科学文献数据的检索、收集；

7.协助项目经理组织召开项目例会，记录会议纪要等工作;

8.完成上级经理分配的其他工作。

1.Assisted PM to manage and solve the OHGRA related works;

2.Assisted PM maintain good and effective communication with relevant personnel of OHGRA;

3.Responsible for the application and delivery process to OHGRA;

4.To coordinate administrative affairs in the clinical department;

5.Assisted in clinical registration affairs tasks;

6.Assisted in sorting out and collecting on clinical trial documents and scientific literature data;

7.Assisted the project manager in organizing and holding regular meeting of the project and taking meeting minutes;

8.Complete other tasks assigned by the superior manager.

任职条件:

1.医学、药学、护理、生物类等相关专业；

2.本科或以上学历，有1 - 2年与工作职责直接相关的工作经验；

3.1-2年的临床行政/助理经验或相关工作经验及相关行业背景，或同等的教育和经验的结合，足以成功地履行工作的基本职责；

4.有国际制药行业资深CTA经验者优先；

5.学习能力强，积极主动、优秀的沟通能力；

6.对这个职位有很强的驱动力；

7.临床试验的基本知识。有处理和校对数字数据的能力；

8.计算机素养:计算机能力强:熟练使用Microsoft Office办公软件(Word、Excel、PowerPoint等)。

1.Academic / Professional qualification in medicine, nursing, biology or related majors

2.Bachelor's degree or above with 1 to 2yearsexperience directly related to the duties and responsibilities specified.

3.1-2 years Clinical Admin/assistant experience or relevant working experience, Industry background is required, or an equivalent combination of education and experience sufficient to successfully perform the essential duties of the job;

4.Experienced CTAs in global pharma will be highly preferred;

5.Quick learner and active team member, excellent communication skills;

6.Strong motivation for this position;

7.Basic knowledge of Clinical Trail. Aptitude for handling and proofreading numerical data;

8.Computer literacy: Strong computer skills: proficient with Microsoft Office (Word, Excel, PowerPoint etc.).