Are you an experienced Clinical Research Associate looking to join a dynamic and growing clinical research organisation? We are seeking a CRA II to manage investigative sites across Spain, ensuring clinical trials are conducted in accordance with study protocols, ICH-GCP, and applicable regulatory requirements. Key Responsibilities * Conduct site qualification, initiation, monitoring, and close-out visits. * Ensure patient safety, data integrity, and protocol compliance. * Perform source data verification and review study documentation. * Manage site relationships and provide ongoing support to investigators and study staff. * Assist with ethics committee and regulatory submissions where required. * Monitor investigational product accountability and site performance. * Maintain Trial Master File (TMF) documentation and support query resolution. * Collaborate with cross-functional study teams to ensure successful trial delivery.



About You * Life Sciences degree or equivalent experience, plus recognized CRA training. * Minimum 4 years' clinical research experience. * Minimum 2 years' monitoring experience as a CRA. * Strong knowledge of ICH-GCP, clinical trial regulations, and site management. * Fluent in Spanish and English languages, Portuguese is desirable * Excellent communication, organisation, and problem-solving skills. * Ability to work independently and manage multiple priorities. * Valid driver's license and willingness to travel up to 75%. What We Offer * Home-based flexibility. * Opportunity to work on international clinical trials. * Collaborative and supportive team environment. * Competitive salary and benefits package.

📌 Clinical Research Associate II (Madrid)
🏢 Linical
📍 Madrid