03 set - Milano
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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 incentives
Health and wellbeing programmes including medical, dental, and vision coverage
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways
Coordinate monitoring activities at clinical trial sites to ensure protocol adherence and timely issue resolution
Assist in preparing and reviewing regulatory documents to ensure GCP compliance
Collaborate with cross-functional teams to support trial sites throughout the study lifecycle
Track site performance metrics, analyze data, and generate reports to improve efficiency
Participate in training initiatives and mentor junior staff in clinical trial management
Bachelor's degree in life sciences, healthcare administration, or clinical research
Experience in clinical research, site management, or monitoring with knowledge of clinical trial processes and GCP
Strong organizational and project management skills with ability to manage multiple priorities
Excellent analytical skills and attention to detail
Exceptional communication and interpersonal skills for working with site personnel and cross-functional teams In this SMA II role, you support the management and monitoring of clinical trial sites to ensure adherence to study protocols, regulatory re...
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