Key responsibilities: • study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties

(LSFR) Clinical Trials Assistant - Based The Netherlands 5 juli 2010

vacature in Amsterdam

Lead (CTL) and Clinical Research Associates (CRAs) with accurately updating and maintaining clinical ... Lead (CTL) and Clinical Research...

(LSFR) Clinical Trials Assistant - Based in Breda, The Netherlan 16 juli 2010

vacature in Amsterdam

Lead (CTL) and Clinical Research Associates (CRAs) with accurately updating and maintaining clinical ... Lead (CTL) and Clinical Research...

Medical Science Liaison (MSL) 12 juli 2010

vacature in Netherlands

, CGR richtlijnen and SOPs A good understanding of clinical research and the ability to critically ... , CGR richtlijnen and SOPs A good...

CRA met minimaal 1 jaar werkervaring 13 juli 2010

vacature in Regio Utrecht

Clinical Research Associate/CRA zoeken wij de volgende achtergrond:- HBO/WO werk en denkniveau (verkregen ... Clinical Research Associate/CRA...

Promotional Quality Officer 7 juli 2010

vacature in Netherlands

pharmaceutical industryGood knowledge of standards for clinical research and research methodologyAble to work in ... pharmaceutical industryGood...