Pharmacovigilance Specialist The Pharmacovigilance Specialist will play a key role in ensuring the safety of our patients by implementing local pharmacovigilance strategies that meet regulatory requirements and company policies. - Local pharmacovigilance management: Supervise local programs for pharmaceuticals, vaccines, and clinical studies, meeting local regulation and internal GSK policies. - Regulatory relationship management: Report adverse events to INVIMA and serve as liaison during regulatory inspections. - Culture and training: Train internal and external personnel on reporting adverse events, promoting compliance with human safety policies. - Cross-functional coordination: Collaborate with quality, customer service, and medical information departments to manage patient safety complaints, inquiries, and risks. - Document management and audit: Ensure proper record-keeping, lead periodic controls, and contribute to audits and continuous quality improvement projects. Requirements - Healthcare professional with specialized training in pharmacovigilance and local regulations. - Experience in patient safety systems or pharmacovigilance. - Strong English language skills. - Thorough knowledge of Colombia's healthcare system. - Effective communication skills and proficiency in Microsoft Office tools. About GSK GSK is a global biopharmaceutical company working to improve people's health and wellbeing through innovative science and technology. Our mission is to unite science, talent, and technology to advance healthcare. Our goal is to make GSK a place where people can thrive, feel welcome, valued, and included. A place where they can grow and take care of their wellbeing. We're committed to creating an inclusive workplace where everyone feels empowered to contribute their best work.