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Clinical Research Associate (CRA) - France  

Company managed [?] Still accepting applications
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Posted on : 07 April 2017

Project Description

We are looking for a Clinical Research Associate in France 

Tasks & Responsibilities  
  • Organization, coordination, administrative management and monitoring of clinical trials (phase I – IV), non-interventional studies, medical device studies according to ICH/GCP guidelines 
  • Data review and source data verification 
  • Ensure investigator compliance with protocol, study procedures, regulatory requirements and timelines 
  • Interact directly with clinical sites, including clinical investigators and other health care professionals involved in the clinical study and maintain a positive rapport with each site 
  • Collection of essential documents from site applicable for submission and trial master file 
  • Oversight and support of sites with recruitment and retention strategies and perform motivational visits if needed 
  •  Site management and remote monitoring in order to support investigational sites  
  •  Solve problems and act pro-actively   

Qualifications & Requirements 
  • Medical/ nursing or life science degree 
  • Minimum of 2 years experience in clinical monitoring 
  • Monitoring in different indications and study types; experience with cancer trials or medical devices is preferable 
  • Good knowledge of ICH-GCP guidelines and all applicable local regulations 
  • Excellent organization and communication skills