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Jr Clinical Research Associate

Posted on Jun 12, 2019 by ARCQ

Anderlecht, Brussel, Belgium
Health Care
Immediate Start
Annual Salary
Full-Time
As a Clinical Research Associate you are responsible for: managing clinical trials from start to finish: you carry out pre-study visits, you initiate the trial, you are responsible for routine monitoring and closing visits about the quality standards and timelines obtaining and updating essential documentation in compliance with ICH-GCP, Procedural Documents and local regulations both in a Trial Master File (eTMF) and Investigator Study File (ISF) participating actively in Local Study Team meetings training, supporting and advising investigators and site staff about study-related matters contributing to Investigators meetings initiating, monitoring and closing study sites in compliance with procedural documents. You share information on patient recruitment and study site progress with Local Study Teams being in charge of performance at the site. You proactively identify study-related issues and find the appropriate solutions updating the CTMS system and other systems with data from ...

Reference: 709074527