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 focused on well-being and work-life balance, including various annual leave entitlements, health insurance, retirement planning, and a global employee assistance program.
ICON is dedicated to providing an inclusive and accessible environment for all candidates and is committed to a workplace free of discrimination and harassment.
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
regulatory compliance management
team management skills
clinical trials safety monitoring
global pharmacovigilance regulations
Nice-to-have
cross-functional team collaboration
leadership and training abilities
detail-oriented multitasking
inclusive workplace culture
Key Requirements
8+ years in pharmacovigilance or drug safety
Bachelor’s degree in life sciences or pharmacy
experience with clinical trials or post-marketing surveillance