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Program Manager ICS

ABN Amro - Diemen
and frameworks of the program. Drawing up the value case in collaboration with project sponsor and Finance. Timely start-up (pre-) CRA , CLA, etc. Realize detailed program planning. Drawing up and realizing DOD, approach and
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Clinical research associate

Undisputed Muay via Magnet.me - Amsterdam
associate ( CRA ) Clinical Monitoring Center is op zoek naar een enthousiaste en liefst ervaren CRA . Wat ga je doen? Als Clinical research associate ( CRA ) monitor je of bij het klinisch onderzoek met mensen (WMO-plichtig
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Clinical Trial Coordinator

Icon Plc - Amsterdam
volgens ICH-GCP opvolgt samen met de CRA en het studie-team Jouw verantwoordelijkheden omvatten : archiveren en tracken van essentiële studiedocumenten labels voorzien voor de te onderzoeken medicatie en studiemateriaal
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CRA II in ICON

Icon Plc - Amsterdam
Associate you will be accountable for performance and compliance for assigned protocols and sites in the Netherlands. Under the oversight of the CRA manager you will ensure the compliance of study conduct (according ICH-GCP and

SMA II in ICON

Icon Plc
Similar jobs at ICON CRA Salary Location Chile Department Clinical Operations Roles Location Chile Remote Working Remote Business Area ICON Strategic Solutions Job Categories Clinical Trial
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ICON Careers

Icon Plc - Amsterdam
Diversity, Inclusion & Belonging ICON Cares - ESG Rewards & Benefits Learning & Development Development Opportunities CRA Learning Opportunities Career Journeys Growing your career at ICON Why icon? full service
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Senior CRA

Icon Plc - Amsterdam
you will be responsible for 2-3 studies (depending the number of sites), throughout the Netherlands and will have an average of 6-8 visits/month (this might vary and is given as an indication!) The CRA executes clinical
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Senior CRA - Medical Devices

Icon Plc - Amsterdam
roxanne.bicknell@iconplc.com View my other roles Send me a message Send Cancel About the role This vacancy has now expired. Please see similar roles below... CRA /Senior CRA - Medical Devices Based from Home or
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Clinical Research Associate

Icon Plc - Amsterdam
the CRA manager you will ensure the compliance of study conduct (according ICH-GCP and coutnry regulations, sponsor policies, quality standards and adverse event reporting requirements. Acts as primary site contact and site
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