Clinical Research Associate (CRA) Ref KKS0210082

Responsibilities:
• Ensure the correct implementation (multicenter) clinical trials phase I to IV at home and abroad according to international standard ICH-GCP
• performing duties as part of monitoring (site selection, initiation, Monitoring, close-out)
• Support of the investigators during all stages of study implementation

Requirements:
• Training as a nurse or medical /  Documentations-assistent or student assistant or in graduate /  natural scientist and physician.
• Experience with the assistance of clinical studies and monitoring, knowledge of ICH-GCP guideline, medical knowledge, good computer skills and good spoken English and writing.
• Along with the ability to communicate and work in the team, you possess excellent organizational skills. Responsibility, independence and high quality standards identify your needs. Multi-day trips are not a nationwide problem for you.