Overview Senior CRAs in Spain join an evergreen talent pipeline to support a strategic sponsor in a collaborative, quality-driven environment. You will monitor studies, ensure compliant conduct, and work across cross-functional teams from site setup to study closeout. The role offers home-based flexibility and opportunities to mentor junior staff and engage directly with clients. This is a high-impact position focused on delivering quality clinical data and supporting complex, multi-country trials. Responsabilidades * Monitor progress of clinical studies at investigative sites to ensure adherence to protocol, SOPs, ICH-GCP, and regulations * Coordinate study setup and monitoring activities: identify investigators, regulatory submissions, pre-study and initiation visits * Support trials of varying scope within a CRO/pharma environment, including larger studies * Train and mentor junior staff members * Interact with clients, initiate payments,



and contribute to proposal development and client presentations Requisitos principales * Minimum 5 years of CRA/ SCR A experience in CRO, pharmaceutical, biotechnology, or medical device environment * Experience in IVD, oncology, infectious diseases, and gastrointestinal studies * Proven multi-country monitoring experience in Europe (Germany, France, UK, Denmark) * Domestic travel up to 50–60% (international travel may be required for some roles) * Fluency in Spanish and English; additional languages a plus * Holder of CRA certificate * 4-year college degree or equivalent * calm and thoughtful under pressure * strong preparation and proactive planning * attention to detail * ICH-GCP compliance * regulatory submissions coordination * site monitoring and study management

📌 Senior Clinical Research Associate (Badajoz)
🏢 Precision Medicine Group
📍 Badajoz