ICON seeks a Pharmacovigilance Supervisor to oversee safety monitoring and adverse event reporting for clinical trials and marketed products. The role involves managing day-to-day operations, leading a team, and ensuring compliance with global regulatory standards in a sponsor-dedicated model based in Mexico City.
Responsibilities
Supervise day-to-day pharmacovigilance operations and ensure timely, accurate adverse event reporting
Collaborate with clinical operations and regulatory affairs teams to optimize safety processes
Ensure compliance with integral regulatory requirements and internal standard operating procedures
Manage safety data collection, analysis, and submission to regulatory authorities
Provide leadership and training to pharmacovigilance team on best practices
Requirements
Bachelor's degree in life sciences, pharmacy, or related field
Pharmacovigilance or drug safety experience in clinical trials or post-marketing surveillance
Strong knowledge of global pharmacovigilance regulations and guidelines
Proven leadership and team management capabilities
Strong communication and organizational skills with attention to detail