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
Entry‑level to 1 year of experience in clinical research, including internships, trainee roles, or up to 12 months of onsite monitoring experience
Basic understanding of ICH‑GCP guidelines and clinical trial processes
Strong attention to detail, willingness to learn, and ability to follow established procedures and documentation standards
Fluency in German and English, both written and spoken
Comfortable using clinical systems and tools, with openness to travel as required for site visits.

Clinical Research Associate I / II

Key skills