Clinical Research Associate II – Germany & Netherlands

About the role

Avania is seeking a Clinical Research Associate II (CRA II) to support clinical trials across the Netherlands and Germany. The CRA II will ensure patient safety, data integrity, and compliance with study protocols, ISO14155, and ICH‑GCP standards. This role offers the opportunity to work independently while collaborating with senior colleagues.

Key responsibilities

• Conduct regular site monitoring visits and other study‑related visits (feasibility, site setup, close‑out).
• Verify that trial data are accurate, complete, and sourced from original documents.
• Manage multiple active studies, balancing several protocols and sites simultaneously.
• Travel frequently to sites, adapting workload based on study needs.
• Support senior team members by handling site‑facing tasks, especially in Germany.

Required profile

• Prior experience as a Clinical Research Associate at a level comparable to CRA II.
• Strong German language proficiency.
• Residence in the Netherlands is preferred; candidates based in Germany are also considered.
• Practical, adaptable approach to site management and ability to handle various visit types.

Required skills

• Knowledge of ICH‑GCP guidelines.
• Familiarity with ISO14155 standards.
• Experience in clinical trial monitoring and site management.