Senior Pharmacovigilance Associate

Senior Pharmacovigilance Associate role at a global contract research organization, responsible for managing drug safety activities, adverse event reporting, and regulatory compliance in a remote position based in Santiago, Chile.

Responsibilities

• Lead collection, evaluation, and processing of adverse event reports per regulatory guidelines
• Conduct data analysis to identify safety trends and potential signals requiring investigation
• Prepare and submit periodic safety update reports and regulatory documentation
• Collaborate with medical teams to assess clinical relevance of adverse events
• Oversee pharmacovigilance database maintenance, integrity, and compliance

Requirements

• Bachelor's degree in scientific or healthcare-related discipline
• Extensive pharmacovigilance or drug safety experience with regulatory knowledge
• Demonstrated ability to manage adverse event reporting and signal detection processes
• Strong analytical and critical thinking skills for complex data interpretation
• Proficiency in pharmacovigilance databases and Microsoft Office Suite
• Excellent cross-functional communication and collaboration abilities
• Willingness to travel approximately 15% as required