Closing Date: 08 Dec 16
Salary (£): Competitive
Our Clinical Research Associates manage all aspects of site monitoring responsibilities for Clinical trials, according to Covance Standard Operating Procedures, ICH guidelines and GCP, including Pre-study qualification, Initiation Meetings, Routine, Interim monitoring Visits and Close-out Visits.
The CRA may serve as Lead CRA and a resource for internal and external clients.
In order to be considered you must have the following:
THERE IS NO BETTER TIME TO JOIN US!
Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.
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