healthcare
Posted 3 weeks agoClinical Research Associate II based in Germany
at Fortrea
Munich, GermanyRemote
Responsibilities
- 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. Required
Requirements
- experience who are eager to further develop their skills in a structured and supportive environment.
- 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
- Qualifications : University or college degree in life sciences, nursing, pharmacy , or a related field; relevant internships or equivalent
- 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.
- We welcome applications from early‑career candidates who are motivated to build a career in clinical research and grow with Fortrea.
Additional details
- As a Clinical Research Associate II, you will take the next step in your clinical research career, supporting the successful delivery of clinical trials under the guidance of experienced colleagues.
- This role is suited for professionals with at least one year of onsite monitoring
- 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
- 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.