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
Job Summary
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.
Embrace and contribute to ICON’s culture of quality and process improvement with a focus on enhancing processes, systems and tools, adding value to our business and meeting or exceeding client needs.
Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Matching Summary
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.
Skills & Requirements
Must-have
ICON SOPs/WPs
ICH/GCP
regulatory processes
critical document package
site activation tasks
quality control review
Nice-to-have
foster an inclusive environment
culture of quality
process improvement
enhancing processes, systems and tools
adding value to our business
meeting or exceeding client needs
Key Requirements
Bachelor’s Degree preferably in Life Sciences
Minimum of 2 years’ experience
Knowledge of local and/or international regulatory processes
Ability to read and understand clinical protocols
Strong attention to detail and organizational skills
Ability to work independently
Excellent communication skills both in English and Spanish