HGR Specialist人类遗传办专员

公司部门: Clinical Development

工作地点:北京

发布日期:2022-03-10

招聘人数:1人

职位类型:生物制药/医疗器械

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.).

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