北京招聘

Responsibilities:

- Under the direction of senior staff, assist with the formatting and compilation of regulatogry submissions through such tasks as entering into TOCs and creating Tabs and submission labels;
- Provide support assistance to senior staff in the upkeep of regulatory authority submission and correspondence log;
- Generate routine submission cover letters to regulatory authorities and clients;
- Track, inventory, and organize individual components of regulatory submissions;
- Perform document acceptability checks of submission components;
- Liaise with copy center in the generation of submissions;
- Provide support assistance to senior staff in the oversight, final preparation and generation of submission documents;
- Update status reports and tracking sheets of ongoing and pending regulatory projects with input provided by senior staff;
- Organize shipping of documentation to clients, regulatory authorities, and/or within Covance;
- Perform other activities as required by management.

Education/QualificationsUniversity/College Degree, prefered Bachelor's Degree in Life Sciences

Covance is one of the world’s largest and most comprehensive drug development services companies with more than 10,000 employees in 60 countries. Through its nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.

Well come to our online job pool to dig out more opportunities at:
http://careers.covance.cn/