pWorldwide Clinical Trials is seeking a Clinical Operations Site Management professional to join our integral team from Spain. You will ensure data quality from study sites and support timely regulatory submissions, while maintaining documentation such as IRB approvals and informed consent where needed. /ppWorking with experts across therapeutic areas, you will help identify potential sites, conduct feasibility activities, and collaborate with sponsors to solve complex challenges in a supportive, /p #J-18808-Ljbffr