Pharmacovigilance Director
ICON · Sao Paulo, Brazil
The apply link worked recently (not employer-confirmed).
Role summary
This director-level role oversees pharmacovigilance and drug safety operations for a clinical research organization's sponsor-dedicated portfolio in São Paulo. Responsibilities include developing safety strategies, leading cross-functional teams, analyzing adverse event data, and maintaining regulatory compliance throughout the product lifecycle. The position requires extensive pharmacovigilance experience, strong leadership abilities, and expertise in safety reporting systems.
What they're looking for
- Bachelor's degree in scientific or healthcare discipline; advanced degree preferred
- Extensive pharmacovigilance or drug safety experience with regulatory knowledge
- Strong leadership skills and cross-functional team management in matrix environments
- Proficiency in data analysis, pharmacovigilance databases, and safety reporting systems
- Excellent communication and stakeholder management abilities
What you'll be doing
- Lead pharmacovigilance strategy development and implementation ensuring regulatory compliance
- Oversee drug safety delivery across assigned portfolio and develop team capabilities
- Assess safety data with cross-functional teams to identify product-associated risks
- Analyze and interpret safety data to inform risk mitigation strategy decisions
- Provide strategic guidance on adverse event reporting and safety monitoring practices
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.