Senior CRA – TOP Global CRO

September 7, 2012 by
Filed under: Clinical Research 

Senior CRA Italy
Milan Office Based or Home based available

Leading global pharmaceutical service provider is looking for experienced Clinical Research Associates with at least 3 to 5 years of experience in monitoring to join their Clinical Development Department on a permanent basis to provide high quality service to the sites and to the best international sponsors.
You will be in charge of the monitoring activities, ensuring and assuring the quality of the data collected on site according to ICH-GCP, SOP and study protocol. You will have responsibilities of Site Management, identifying, selecting, initiating and closing-out investigational sites and acting as liaison between study site and in-house team. You will also be in charge of the Study Management, working independently and proactively to coordinate all necessary activities required to set up and monitor a study.
Qualifications:
* University degree in a science related field or certified health care professional or equivalent experience
* D.M. 2011 Certification
* Experience as CRA in clinical development phase II – IV
* In depth knowledge of ICH-GCP, EU and FDA requirements
* Excellent Italian and English language skills (spoken and written)
* Willingness & ability to travel (approx. 50%)
* Capability to work in a team
My Client can offer a competitive salary and benefits package and will support individual as well as professional development in one of the most important global companies in the Industry.
To apply, forward your CV to Sergio.carito@secpharma.com
Call Sergio Carito on + 44(0)207 255 66 00 for further information and a confidential discussion of this opportunity.
Sergio Carito
Consultant Biotech, Pharmaceutical, Healthcare & CRO Division
Italy and Europe
Tel: +44 (0) 207 255 6665
sergio.carito@secpharma.com
http://uk.linkedin.com/in/sergiocarito

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