Support preparation, process and tracking of regulatory and site level critical documents and of site activation tasks required for study site activation
Job Summary
Support preparation, process and tracking of regulatory and site level critical documents and of site activation tasks required for study site activation.
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.
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
Support preparation, process and tracking of regulatory and site level critical documents and of site activation tasks required for study site activation.
Skills & Requirements
Must-have
ICON SOPs/WPs knowledge
ICH/GCP knowledge
Regulatory document processing
Site activation tasks
Critical Document Package assembly
TMF document QC
Nice-to-have
Culture of quality and process improvement
Enhancing processes, systems and tools
Client needs focus
Proactive follow through
Key Requirements
Minimum 2 years clinical study start up experience
Bachelor's Degree in Life Sciences
Local and/or international regulatory processes knowledge