ICON is seeking a Clinical Site Associate for a hybrid role based in the Czech Republic, focused on supporting site management activities in clinical trials. The ideal candidate should possess relevant experience in clinical research or administration and have strong organizational and communication skills
Job Summary
As a Clinical Site Associate at ICON, you will support site management activities and ensure that clinical trials are conducted efficiently, compliantly, and to the highest quality standards.
You will contribute to scientific operations activities, taking responsibility for your deliverables and working collaboratively.
In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance.
Matching Summary
Match Score: 85
ICON is seeking a Clinical Site Associate for a hybrid role based in the Czech Republic, focused on supporting site management activities in clinical trials. The ideal candidate should possess relevant experience in clinical research or administration and have strong organizational and communication skills.
Skills & Requirements
Must-have
support site activation activities
maintain site information
assist CRAs and project teams
coordinate site visit logistics
ensure accurate document filing
collaborate on site payments
contribute to process improvement
Nice-to-have
customer-focused approach
adapt to changing priorities
Key Requirements
Bachelor's degree or equivalent experience
Initial experience in clinical research or regulated environment