Operations Specialist 1

As an Operations Specialist 1, you will review, assess, and process safety data from various sources, ensuring compliance with regulatory standards and internal guidelines. You will work under the guidance of senior team members to support pharmacovigilance activities, including adverse event reporting, medical reviews, and database management. Key Responsibilities ✔ Process safety data in compliance with SOPs, regulatory guidelines, and project requirements. ✔ Perform pharmacovigilance activities such as: Collecting and tracking Adverse Events (AEs) Database entry, coding AEs and products Writing narratives and handling literature-related tasks ✔ Ensure high-quality standards and meet productivity & delivery timelines. ✔ Maintain 100% compliance with training and documentation. ✔ Support team mentoring and departmental initiatives. ✔ Liaise with cross-functional teams (clinical, data management, project managers). ✔ Assist in medical reviews of non-serious AEs/ADRs (if required).

IQVIA is a global leader in providing advanced analytics, technology solutions, and clinical research services to the life sciences and healthcare industries. With a focus on accelerating medical innovations, IQVIA helps improve patient outcomes worldwide. The company offers intelligent insights and data-driven solutions to pharmaceutical, biotech, and healthcare organizations.