北京招聘

Responsibilities/Duties

- To Be Completed by Hiring Manager - Assist in the preparation of routine submissions filed to Regulatory Authorities (e.g.: INDs,
CTAs, NDAs, NDSs, MAAs or CTDs).
- Contribute to the preparation of submissions to Health Authorities by reviewing/summarizing
scientificlresearch documents.
- Assist in the coordination, collection and organization of information required by Regulatory
Authorities
- Interact with the Copy Center or equivalent as necessary for the publishing of submissions.
- Maintain knowledge and awareness of regulations and guidelines pertaining to drugs and
biologics.
- Monitor compliance with regulatory requirements in relation to assigned projects.

Education/Qualifications Bachelor's Degree in Life Sciences or equivalent

Experience - 2-5 years regulatory affairs experience
- Experience in the pharmaceutical industry

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/