Pharmacovigilance Specialist

Job Overview

Handle safety data and information, distribute reports to internal and external parties following regulations, SOPs, and guidelines with support from senior team members.

Key Responsibilities

Complete assigned trainings on time. Process safety data following regulations, SOPs, and project requirements. Perform Pharmacovigilance activities including collecting and tracking Adverse Events (AE), database entry, coding AE and products, writing narratives, and literature-related activities. Meet quality, productivity, and delivery standards. Comply with all project-related processes and activities. Acknowledge all necessary SOPs and ensure timely and documented training. Create, maintain, and track cases as per the project plan. Identify and report quality issues to senior team members. Demonstrate problem-solving capabilities. Collaborate with functional team members and health care professionals to address project-related issues. May liaise with clients regarding daily case processing activities. Mentor new team members if assigned. Attend project meetings and provide feedback on any challenges or successes. Lead or support department initiatives. Ensure 100% compliance with all people practices and processes. Depending on the project, may perform medical review of non-serious AEs and ADRs.

Qualifications

High School Diploma or equivalent in a scientific or healthcare discipline required. Bachelor's degree in life sciences or related field and up to 3 years of relevant experience, including up to 1 year of Pharmacovigilance experience preferred. Good knowledge of medical terminology, safety databases, clinical research regulatory requirements, and Microsoft Office. Excellent attention to detail, organizational skills, and communication skills. Self-motivated, flexible, and able to work independently. Ability to multi-task, meet deadlines, manage priorities, and adapt to changing demands. Willingness to learn new skills and ability to work as a team player. Regular sitting for extended periods, occasional travel, and flexibility to operate in shifts may be required.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at

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