Cra 2 - Romania

Here in Fortrea we are looking for an experienced CRA to join our miltisponsor team. **Responsibilities:** * Conduct site monitoring visits (initiation, routine, close-out) in line with SOPs, ICH-GCP, and study requirements * Ensure patient safety and protocol compliance, including informed consent and eligibility verification * Perform source data verification, resolve queries, and maintain high data quality and integrity * Maintain site documentation (ISF/eTMF) and ensure audit readiness at all times * Manage investigational product accountability and site supplies in line with protocol requirements * Collaborate with study teams to deliver milestones, prepare reports, and support timelines **Requirements:** * Degree in Life Sciences, Nursing, or related field (or equivalent experience) * Minimum 2 years of independent clinical monitoring experience * Strong knowledge of ICH-GCP, clinical trial processes, and regulatory requirements * Ability to work independently, with good organisation and problem-solving skills * Experience with eClinical systems (e.g. CTMS, eCRF) and solid MS Office skills * Fluency in English and Romanian languages; willingness to travel (~60%) Learn more about our [EEO & Accommodations request here](https://careers.fortrea.com/us/en/eeo-and-accommodations).