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CRA II - Multi-Therapeutic - Madrid or Barcelona

Post updated: 23/11/2014


The Clinical Research Associate is accountable and responsible for all aspects of site management and monitoring activities for assigned applicable Phase I and all Phase II-IV clinical Investigator sites within the approved Clinical Development Plan (CDP). These global, complex studies are conducted within the standards set by the company, according to Good Clinical Practices and applicable regulatory and legal requirements. The CRAworks in close collaboration with the Country Lead Monitorand Study Lead Monitor for internally monitored and outsourced clinical trials. Responsibilities Managing Investigator site and site activities and monitoring site data ...

Submission Deadline: 06/12/2014
Contact email: http://eu.experteer.com/account/signup_now/expatica_com/2869296







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