Clinical Research Associate II - Spain

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.