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.

ResponsabilidadesMonitor progress of clinical studies at investigative sites to ensure adherence to protocol, SOPs, ICH-GCP, and regulationsCoordinate study setup and monitoring activities: identify investigators, regulatory submissions, pre-study and initiation visitsSupport trials of varying scope within a CRO/pharma environment, including larger studiesTrain and mentor junior staff membersInteract with clients, initiate payments,



and contribute to proposal development and client presentations Requisitos principalesMinimum 5 years of CRA/ SCR A experience in CRO, pharmaceutical, biotechnology, or medical device environmentExperience in IVD, oncology, infectious diseases, and gastrointestinal studiesProven 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 plusHolder of CRA certificate4-year college degree or equivalentcalm and thoughtful under pressurestrong preparation and proactive planningattention to detailICH-GCP complianceregulatory submissions coordinationsite monitoring and study management

📌 Senior Clinical Research Associate (Madrid)
🏢 Jobrapido
📍 Madrid