In this SMA II role, you support the management and monitoring of clinical trial sites to ensure adherence to study protocols, regulatory requirements, and GCP. You coordinate monitoring activities, assist in regulatory document preparation, and collaborate with cross-functional teams. You track site performance and provide reports to improve site management. You also participate in training initiatives and mentor junior staff, contributing to a values-driven, patient-focused research environment.Competitive base salary and performance related incentivesHealth and wellbeing programmes including medical, dental, and vision coverageRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysCoordinate monitoring activities at clinical trial sites to ensure protocol adherence and timely issue resolutionAssist in preparing and reviewing regulatory documents to ensure GCP complianceCollaborate with cross-functional teams to support trial sites throughout the study lifecycleTrack site performance metrics, analyze data, and generate reports to improve efficiencyParticipate in training initiatives and mentor junior staff in clinical trial managementBachelor's degree in life sciences, healthcare administration, or clinical researchExperience in clinical research, site management, or monitoring with knowledge of clinical trial processes and GCPStrong organizational and project management skills with ability to manage multiple prioritiesExcellent analytical skills and attention to detailExceptional communication and interpersonal skills for working with site personnel and cross-functional teamsIn this SMA II role, you support the management and monitoring of clinical trial sites to ensure adherence to study protocols, regulatory re...
J-18808-Ljbffr

📌 Site Management Associate II (Milano)
🏢 Experteer Italy
📍 Milano