Senior Clinical Research Associate – Per un 2013 di successo

December 21, 2012 by · Comments Off on Senior Clinical Research Associate – Per un 2013 di successo
Filed under: Clinical Research 

Senior CRA Italy

Milan Office Based or Home based available

Global CRO is seeking a talented Senior CRA with at least 4 years of solid experience in monitoring activities to join them on a permanent basis. 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 Life Science Degree

* D.M. 2011 Certification

* Experience as CRA in 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%)

* Teamwork

My Client can offer a competitive salary and benefits package, the best training in the industry and will support individual as well professional development in one of the most important global companies in the Clinical Research.

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

Il lavoro che hai sempre desiderato nella ricerca clinica

December 26, 2011 by · 8,790 Comments
Filed under: Clinical Research, Regulatory Affairs 

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