长沙招聘

At Covance, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world.

Our commitment to this mission has resulted in Covance’s impressive history of company stability and growth. We’ve achieved these results by fostering a work environment that encourages, develops and leverages our team’s capabilities.
Covance’s ongoing success offers team members unsurpassed growth and career development opportunities. There’s no better time to join us!


Responsibilities/Duties:

-Data entry
-Filing and archiving of study documents
-Study drug management
-IRB submission
-Management of patient visit
-Coordinating CRA’s monitoring visit to the site
-Support AE/SAE reporting
-Site contact /communication
-Assistance to audits
-Data confidentiality
Note: CRC should not work on the studies that are monitored by Covance CRAs


Requirements:

- College or Bachelor degree in life science, medical, nursing or other relevant majority;
- clinical research coordinator experience preferred

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/