Monitor clinical trials and ensure compliance with regulations, GCP, and SOPs. Conduct site qualification, initiation, interim, and closeout visits. Train site staff and proactively manage site performance. Qualifications: Health-related degree with clinical research monitoring experience. Knowledge of ICH/GCP guidelines and applicable regulations. Strong planning, analytical, and communication skills. Remote based in Madrid with travel to study sites. Dynamic environment with competing projects and deadlines. AbbVie AbbVie discovers and delivers innovative medicines and solutions across immunology, oncology, and neuroscience. It is a global biopharmaceutical company committed to integrity, innovation, and transforming lives. #J-18808-Ljbffr
Clinical Research Associate I (Fully Remote) in workfromhome at Unknown Company
This position is listed as full time and able to be worked remotely.