Clinical Research Associate based in Germany or in Austria

Support the management of clinical trial sites in compliance with Fortrea SOPs, ICH‑GCP, study protocols, and sponsor requirements, with appropriate supervision.

Assist in the preparation and conduct of site monitoring activities, including site initiation, routine monitoring, and close‑out visits, ensuring patient safety and protocol adherence.

Perform source data verification (SDV), support query resolution, and review eCRFs to help ensure data quality and completeness.

Maintain and update essential trial documentation in eTMF and sponsor systems to support inspection readiness.

Support investigational product (IP) tracking and accountability checks in collaboration with the study team.

Collaborate with cross‑functional teams and escalate issues appropriately, contributing to site performance, quality, and timelines.

University or college degree in life sciences, nursing, pharmacy, or a related field; relevant internships or equivalent experience will be considered.