Location: Munich, Germany
Closing Date: 16 Mar 17
Salary (£): Competitive
Do you know Covance is one of world´s leading Contract Research Organization? For example, our Clinical Development teams have supported the development of one-third of all prescription medicines in the market today and of 47 out of the 50 best-selling oncology drugs.
Can you bring your drive to our cutting-edge clinical projects?
The work we do at Covance impacts the lives of millions of people around the world… so could you too as our next:
Start-up Specialist office based in Munich. We look for someone with background in Ethics Committees Submissions.
If you chose the Submissions path, you will work with investigative sites to collect the required investigator and regulatory documents to perform clinical trials in the DACH region, and ensuring that the documents meet the specifications required by local regulations, EU Clinical Trial Directive, ICH-GCP, FDA regulations and the study sponsor.
Education and qualifications:
Covance is committed to diversity in the workplace and is an equal opportunity employer. Your confidentiality and privacy are important to us.
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