[Hiring] Unblinded Clinical Research Associate @Fortrea

Role Description

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.

Qualifications

• 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.

Benefits

• Opportunity to work in a sponsor-dedicated environment on innovative studies.
• Structured onboarding and continuous development programs.
• Flexible working model supporting work-life balance.
• Access to global career growth opportunities within clinical operations.
• Inclusive and collaborative culture with employee resource groups and wellbeing initiatives.