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Pharmacovigilance Supervisor role at ICON plc, a world-leading healthcare intelligence and clinical research organization. The role involves overseeing the safety monitoring and reporting of adverse events related to clinical trials and marketed products, contributing to patient safety and regulatory compliance.
Job Responsibility:
Supervising the day-to-day pharmacovigilance operations, ensuring timely and accurate reporting of adverse events
Collaborating with cross-functional teams, including clinical operations and regulatory affairs, to optimize pharmacovigilance processes
Ensuring compliance with global regulatory requirements and internal standard operating procedures for safety reporting
Managing safety data collection, analysis, and submission to regulatory authorities
Providing leadership and training to the pharmacovigilance team, ensuring adherence to best practices in safety monitoring
Requirements:
Bachelor’s degree in life sciences, pharmacy, or a related field
High level of English proficiency
Based on Brazil
Experience in pharmacovigilance or drug safety, with a focus on clinical trials or post-marketing surveillance
Strong knowledge of global pharmacovigilance regulations and guidelines
Excellent communication, leadership, and organizational skills, with the ability to manage a team effectively
Detail-oriented with the ability to manage multiple tasks and ensure accuracy in safety reporting
What we offer:
Various annual leave entitlements
A range of health insurance offerings to suit you and your family’s needs
Competitive retirement planning offerings
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments