CRA (Clinical Research Associate)

• Monitor the investigator sites to ensure that the study is being conducted in accordance with the trial protocol, ICH GCP, SOPs/WIs and all applicable regulatory requirements, and process the required documentation
• Ensure that high quality data is generated
• Assist CML/CRA Manager in the implementation of trials to ensure the study timeline and budget are kept

The qualifications required for this challenging position are as follows; 
 

• University degree in Pharmacy, Biology, Chemistry, Genetics, Medicine or a related field
• Min. 1-2 years of CRA experience within a pharmaceutical company / CRO
• Competency in using Microsoft Office tools
• Fluency in English
• Excellent communication skills together with planning and organization ability
• Male candidates should complete their military obligation