Clinical Research Associate II based in Germany

Clinical Research Associate I or II (CRA I / CRA II) : Be the connection between science and solutions. As a Clinical Research Associate I or II, you will take your first or next step into clinical research, supporting the successful delivery of clinical trials under the guidance of experienced colleagues. This role is well suited for early‑career professionals, including candidates coming from internships or with up to 1 year of onsite monitoring experience, who are eager to learn and grow in a structured, supportive environment. You will contribute to the execution of clinical studies across a variety of therapeutic areas, including Oncology, Dermatology, Respiratory, Cardiology, and Diabetes, gaining broad exposure and hands‑on experience while developing your monitoring skills. This role is for upcoming future opportunities that may arise at Fortrea. Key Responsibilities 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 elevate issues appropriately, contributing to site performance, quality, and timelines. Required Qualifications University or college degree in life sciences, nursing, pharmacy, or a related field; relevant internships or equivalent experience will be considered. 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. Why Join Us? Grow your clinical research career in a structured and supportive environment with clear development pathways and mentoring. Gain hands‑on exposure to global clinical trials and multiple therapeutic areas while building strong foundational CRA skills. Benefit from formal training programs, modern clinical systems, and continuous learning opportunities. Enjoy a flexible work model, competitive benefits, and a culture that values collaboration, quality, and well‑being. We welcome applications from early‑career candidates who are motivated to build a career in clinical research and grow with Fortrea. If you are curious, detail‑oriented, and eager to make an impact on patients’ lives, we encourage you to apply. Learn more about our EEO & Accommodations request here. #J-18808-Ljbffr Fortrea