In a nutshellPosition: Clinical Study CoordinatorLocation: Madrid, HibridExperience: 4+ years in international clinical trial coordinationWant to know more?mAbxience is a global biopharmaceutical company committed to innovation and excellence in the development and manufacturing of biotechnological medicines. We operate with a strong focus on quality, regulatory compliance, and scientific rigor to improve patient outcomes worldwide.What are we looking for?- Oversee and ensure the proper execution and follow-up of clinical trials, managing CROs and vendors to meet timelines, quality standards, and regulatory requirements.- Design and manage clinical trial plans, identifying risks and implementing corrective actions.- Coordinate site and investigator selection, budget management, and vendor contracts.- Ensure compliance with GCP, FDA, EMA, ICH guidelines, and internal procedures.- Manage regulatory documentation and submissions, maintaining audit readiness.- Supervise clinical trial monitoring, investigational product handling, and patient recruitment strategies.- Collaborate with pharmacovigilance teams to ensure timely reporting and management of safety events.- Support quality management through monitoring reports, deviation handling, and protocol amendments.- Maintain effective communication with internal teams, CROs, investigators, and regulatory authorities.What do you need?