• 招聘类型：社招
• 工作性质：全职

职位描述

Key responsibilities:

• Manage external CRO's and vendors to support preclinical development programs, and to provide scientific and operational guidance;
• Co-ordinate projects across teams and projects, including active problem solving with other team members and other members of company's leadership team;
• Serve as an internal preclinical drug safety expert for positive, goal-centric behaviors and take a proactive approach to resolve scientific problems and challenges;
• Review preclinical study reports;
• Prepare and edit preclinical documents for regulatory submission;
• Participate in discussion with regulatory agencies to obtain feedback on preclinical programs;
• Maintain a current understanding of regulatory requirements and guidance;

任职条件

Key requirements:

• Master or PhD is required in relevant field (Biology, Pharmacology, Toxicology, Clinical Medicine);

Preference will be given to people having 3+ year experience as Study Director or Project Manager in preclinical development in GLP compliance industry.

职位要求

• 学历要求：硕士
• 工作经验：3年
• 外语要求：不需要

公司福利

• 五险一金 
• 餐饮补贴 
• 交通补贴 
• 补充公积金 
• 补充医疗保险 
• 生日福利 
• 年节福利 
• 年度体检