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Clinical Research Associate (CRA) - France  

Company managed [?] Still accepting applications

Posted on : 04 April 2017

Project Description

We are looking for a Clinical Research Associate in Paris, 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