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.
Supervising the day-to-day pharmacovigilance operations, ensuring timely and accurate reporting of adverse events.
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
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 operations
adverse event reporting
regulatory compliance
safety data management
team leadership
Nice-to-have
fostering inclusive environment
driving innovation and excellence
patient safety focus
work life balance opportunities
Key Requirements
Bachelor's degree in life sciences, pharmacy, or related field
Experience in pharmacovigilance or drug safety
Strong knowledge of global pharmacovigilance regulations
Ability to manage a team effectively
Detail-oriented with ability to manage multiple tasks