As a Site Specialist II at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contribute to efficient study start-up and maintenance
Job Summary
As a Site Specialist II at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contribute to efficient study start-up and maintenance.
Support preparation, process and tracking of regulatory and site level critical documents and of site activation tasks required for study site activation in accordance with ICON SOPs/WPs, Sponsor SOPs, applicable regulations/guidelines and the principles of ICH/GCP.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.
Matching Summary
As a Site Specialist II at ICON, you will independently manage a range of site support activities, acting as a key operational contact for sites and contribute to efficient study start-up and maintenance.
Skills & Requirements
Must-have
Site support activities
Regulatory and site level documents
Study site activation
ICH/GCP compliance
Critical Document Package assembly
Trial Master File (TMF) QC
Nice-to-have
Culture of quality and process improvement
Proactive, service-focused mindset
Collaborate effectively with cross-functional teams
Enhancing processes, systems and tools
Key Requirements
Bachelor's degree in life sciences, healthcare, business, or related field
3-6 years of experience in Clinical Research
Experience in site support or clinical administration
Good understanding of clinical trial processes, GCP