As a Supervisor, Pharmacovigilance at ICON, you will play a pivotal role in overseeing the safety monitoring and reporting of adverse events related to clinical trials and marketed products
Job Summary
As a Supervisor, Pharmacovigilance at ICON, you will play a pivotal role in overseeing the safety monitoring and reporting of adverse events related to clinical trials and marketed products.
ICON offers a range of benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities for you and your family.
At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.
Matching Summary
As a Supervisor, Pharmacovigilance at ICON, you will play a pivotal role in overseeing the safety monitoring and reporting of adverse events related to clinical trials and marketed products.
Skills & Requirements
Must-have
Pharmacovigilance safety reporting operations
Cross-functional team collaboration
Global regulatory compliance
Safety submissions management
Pharmacovigilance team leadership
Nice-to-have
Inclusive and diverse work culture
Employee well-being focus
Strong organizational skills
Detail-oriented multitasking
Key Requirements
8+ years in pharmacovigilance or drug safety
Bachelor’s degree in life sciences or pharmacy
Team management skills
Experience in clinical trials or post-marketing surveillance