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.
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 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 management
Adverse event reporting
Regulatory compliance expertise
Nice-to-have
Leadership and training skills
Collaboration with cross-functional teams
Detail-oriented with multitasking ability
Key Requirements
Bachelor’s degree in life sciences
Experience in pharmacovigilance or drug safety
Strong knowledge of global pharmacovigilance regulations