Descripción de la oferta
Experteer Overview As an SMA II at ICON, you support the management and monitoring of clinical trial sites to ensure protocol, regulatory, and GCP compliance. You will work with cross-functional teams to drive site performance and study deliverables. You help maintain high-quality site activities and mentor junior staff, contributing to overall trial success. This role offers exposure to global oncology and regulatory environments with a mission-driven, collaborative culture.Compensaciones / Beneficios
- Coordinate monitoring activities at clinical trial sites ensuring adherence to study protocols and timely issue resolution
- Assist in preparing and reviewing regulatory documents to ensure GCP and regulatory 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 site management
- Participate in training initiatives and mentor junior staff in clinical trial managementResponsabilidades
- Bachelor in Life Sciences or related field
- Experience in clinical research, site management, or monitoring with knowledge of clinical trial processes and GCP
- Strong organizational and project management skills; able to handle multiplepriorities and deadlines
- Excellent analytical skills and attention to detail
- Exceptional communication and interpersonal skills for building relationships with site personnel and cross-functional teams
- Willingness to travel approximately 25%Requisitos principales
- 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
