跨

朋友你们好，我在帮一家跨国500强的医药R&D中心招聘Clinical Scientist-Virology
，工作地点在北京或者上海。请感兴趣的朋友和我联系，或者请帮忙推荐些这方面的朋
友谢谢。
Email:sun_008@hotmail.com Cell:13439189716

Basic Function:

Provides medical direction of all virology program (especially on HBV and
HCV), plans and implements drug development strategies, clinical trial
designs, safety evaluations and regulatory submissions.

Primary Responsibilities include:
Drafts clinical development plan with the support from clinical project team.
Assesses the global study feasibility, designs and writes local or regional
clinical study protocols, assures protocols will adhere to standard clinical
practices, and develops the case report form with data management team.
Builds strong relationship with KOLs and maintains the contact, selects
suitable clinical consultants for clinical trials or therapeutic area
Works with operation team to resolve the issues during the study conduction,
monitors patients safety in the ongoing clinical studies
Secures the conditions essential for safety, efficacy and medical usefulness
of a drug
Works closely with biostatistics and decides how the resulting data should
be analyzed.
Preparation of abstracts, posters and publications
Represents PDZC in the local and global project teams as core member
Drafts clinical study report, NDA submission and response to regulatory
enquiries.

Qualification and Experience:
M.D. degree with specialty training in Virology, he/she should have
soundable medical knowledge in this therapeutic area.
At least 2-3 years clinical research experience in pharmaceutical industry
or academic institute specifically in virology therapeutic area.
Language: Fluent in English
Other skills and/or competence: good presentation skill, proven ability to
interact well in a team setting.

电子邮件： sun_008@hotmail.com手机： 13439189716
基本职能：
提供医疗方面的所有病毒学计划（尤其是对乙肝病毒和 丙型肝炎病毒） ，规划和实施发展战略的药物，临床试验设计，安全评价和管理意见书。

主要职责包括：
临床发展计划草案的支持下临床项目小组。
评估全球性可行性研究，设计和写入地方或区域 临床研究的协议，确保协议将坚持标准临床做法，以及发展的情况报告的形式与数据的管理团队。
建立强有力的合作关系，选择适合临床顾问，临床试验或治疗领域工程与运营团队合作，解决问题在研究传导， 监测患者安全的正在进行的临床研究保证必不可少的条件，安全性，有效性和医疗作用 药物紧密合作，决定如何产生的数据应进行分析。
编写文摘，海报和出版，临床研究报告，提交新药申请和应对监管查询。


资格和经验：
医学博士学位，接受过培训病毒学，他/她应该有
在这一治疗领域的医学知识。
至少在2-3年的临床研究经验的制药业
或学术研究所的治疗特别是在病毒学领域。
语言：流利的英文
其他技能和/或能力：良好的演讲技巧，
互动能力以及团队合作精神。