Unblinded CRA based in Austria

Join a sponsor-dedicated model supporting cutting-edge clinical trials in DACH. As an unblinded Clinical Research Associate (CRA I or CRA II level) , you will contribute to high-quality clinical research delivery while gaining strong exposure to unblinded study activities in a collaborative global environment.

• →You will perform unblinded monitoring activities in line with ICH-GCP guidelines and applicable regulations, including Investigational Product oversight
• →You will ensure protocol compliance, data integrity, and patient safety at assigned sites
• →You will maintain accurate and complete study documentation, including eTMF and regulatory files
• →You will build strong relationships with site staff, acting as the primary point of contact for site management (pharmacy only)
• →You could contribute to audit readiness and ensure inspection preparedness at site level

• Bachelor’s degree in Life Sciences or related field (or equivalent experience)
• Initial experience in clinical research as a CRA with at least 1 year of monitoring experience
• Understanding of ICH-GCP guidelines and clinical trial processes
• Strong interest and knowledge in unblinded study conduct and Investigational Product management
• Fluency in German and English (written and spoken)
• Willingness to travel within Germany and Austria as required
• Strong organizational skills with attention to detail