北京招聘

A. General Purpose and Scope:
Serves as a Study Director on cardiovascular, central nervous system &/or respiratory safety pharmacology studies in rodents and non-rodents, as described in ICH and GLP regulations/guidelines. Has overall responsibility for the technical conduct of a study as well as for the interpretation, analysis, documentation and reporting of results.

B. Duties and Responsibilities:
? Coordinates efforts of the study team
? Develops protocols and ensures that the protocol, including any changes, is approved and is in compliance with the appropriate SOPs, GLPs, and regulatory agency guidelines
? Reviews cost estimates to ensure that all protocol/amendment driven workscope specifications have been included in the price estimation.
? Monitors financial status of ongoing studies.
? Monitors progress and status of assigned studies. Ensures that all experimental data, including observations of unanticipated responses to the test system, are accurately recorded and verified.
? Directs analysis of data, preparation of reports, ensures compliance with protocol and regulatory requirements, and submits them to the client
? Peer reviews protocols and reports for other Study Directors
? Participates in client visits
? Performs other related duties as assigned

II. Education/Qualifications:
Required:
? Ph.D., DVM, or equivalent degree
? Experience may be substituted for education.

III. Experience:
Required:
? 3-5 years experience

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/