Clinical Research Associate (CRA) – Spain (Madrid or Barcelona area)
We are looking for a Clinical Research Associate (CRA) based in Spain (preferably near Madrid or Barcelona) to join our Global Clinical team being sponsor dedicated full-time.
High-quality, efficient study execution
Strong cross-functional collaboration across global teams
You will play a key role in ensuring patient safety, data integrity, and regulatory compliance across clinical studies, while supporting study acceleration and operational excellence.
Site Monitoring & Data Quality
Perform source data verification (SDV) between CRFs and source documents
Prepare monitoring visit reports, follow-up letters, study memos, and site correspondence
Site Management & Training
Maintain training logs, delegation logs, and site documentation
Collaborate with Trial Operations, Regulatory Affairs, and Contracts & Budget teams
Maintain study milestones in Clinical Trial Management Systems (CTMS)
Bachelor's degree (or equivalent combination of education and experience)
Fluency in Spanish and English (written and spoken)
Minimum 5 years of experience in clinical field monitoring
Medical device experience, particularly in:
Oncology
Endoscopy
Additional language skills (Italian at intermediate level is a plus)
Opportunity to work in a global clinical operations environment
Strong cross-functional collaboration and professional development opportunities
Impactful work supporting high-quality clinical research and patient safety