We are seeking a Supervisor, Pharmacovigilance to oversee the safety monitoring and reporting of adverse events related to clinical trials and marketed products. You will ensure patient safety and regulatory compliance through effective management of pharmacovigilance activities and coordination with cross-functional teams.
Requirements
- Supervising day-to-day pharmacovigilance operations
- Collaborating with cross-functional teams
- Ensuring compliance with global regulatory requirements and internal standard operating procedures
- Managing safety data collection, analysis, and submission to regulatory authorities
- Providing leadership and training to the pharmacovigilance team
Benefits
- Various annual leave entitlements
- Health insurance offerings
- Competitive retirement planning
- Global Employee Assistance Programme
- Life assurance
- Flexible country-specific optional benefits
