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.
You will contribute to ensuring patient safety and regulatory compliance through effective management of pharmacovigilance activities, coordination with cross-functional teams, and maintaining the highest standards of safety reporting.
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
overseeing safety monitoring
adverse event reporting
patient safety and regulatory compliance
global regulatory requirements
internal standard operating procedures
Nice-to-have
foster an inclusive environment
driving innovation and excellence
well-being and work life balance
Key Requirements
8+ years in pharmacovigilance or drug safety
Bachelor’s degree in life sciences, pharmacy, or related field
Team Management skills
Solid experience in pharmacovigilance or drug safety
Strong knowledge of global pharmacovigilance regulations