IQVIA
This position for Pharmacovigilance Analyst supporting LATAM PV operations across PMR, Consulting projects (around 300 project a year) also CES-PSP around 9 projects in LATAM (<6500 adverse events during 2025). The role is critical to ensure timely AE identification and 24-hour reporting to clients, in line with contractual and regulatory requirements, also perform Quality Management, Client Audits, and RFP review. Due to high workload, current 50% capacity, and recent voluntary attrition driven by higher industry salaries, backfilling this position is necessary to maintain compliance, service continuity, audit readiness and client delivery.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.