BrightOwl Loader Loading

Clinical Research Associate Belgium, Germany, Japan,  

Posted on : 10 April 2017

Project Description

Function: You take responsibility for the administration and monitoring of clinical research projects according to our Standard Operating Procedures and the relevant guidelines. You analyze and evaluate clinical data, ensure compliance with protocol and overall clinical objectives; identify, select, initiate and close-out appropriate investigational sites for clinical studies. You monitor the sites in order to ensure that studies are carried out according to the applicable regulations and guidelines. Regular travel is required. Profile: By preference, you have a (para-) medical or scientific degree and at least one (1) year of clinical research experience including monitoring, or at least a minimum of two years experience in pharmaceutical data management or as a study coordinator. You are a detail oriented professional with good negotiation, time management and people skills. Language requirements: Belgium: Fluent in Dutch and English Germany: Fluent in German and English Japan: Fluent in Japanese and English



Find a Job Find Candidates

Most Recent Searches

Most Famous Searches

You might also like