As a Pharmacovigilance Assistant I at ICON, you will play a key role in supporting the collection, documentation, and reporting of safety data related to medications and clinical trials
Job Summary
As a Pharmacovigilance Assistant I at ICON, you will play a key role in supporting the collection, documentation, and reporting of safety data related to medications and clinical trials.
This is a hybrid position, requiring attendance at our Warsaw, Poland or Sofia, Bulgaria office three days per week.
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 opportunities.
Matching Summary
As a Pharmacovigilance Assistant I at ICON, you will play a key role in supporting the collection, documentation, and reporting of safety data related to medications and clinical trials.
Skills & Requirements
Must-have
collection of safety data
documentation of safety data
reporting of safety data
compliance with regulatory requirements
data entry into databases
Nice-to-have
foster an inclusive environment
driving innovation and excellence
work life balance opportunities
inclusion & belonging are fundamental
Key Requirements
Bachelor's degree in life sciences
Basic understanding of pharmacovigilance principles