CRA Level II/Senior CRA (Thessaloniki-based)

Become part of our team as a Clinical Research Associate (Level II) and play a key role in monitoring clinical trials and ensuring regulatory compliance. You will manage site processes, conduct site visits, and support investigational sites. Ideal for candidates with clinical monitoring experience and a background in life sciences or nursing.

Skills

• clinical monitoring
• ich-gcp compliance
• risk based monitoring
• sdr
• sdv
• crf review
• site management
• regulatory compliance
• clinical trial management system
• root cause analysis
• problem solving
• medical terminology
• investigator site initiation
• trial close out
• business writing
• presentation skills
• process improvement
• investigator identification
• trial status tracking
• project team collaboration