Job Overview

This role involves reviewing, assessing, and processing safety data and information, with a strong focus on Medical Information. The data is received from various sources and is distributed to both internal and external parties following applicable regulations, SOPs, and internal guidelines

Key responsabilities

• Review, assess, and process safety data and information, with a strong focus on Medical Information.

• Perform Pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AE)/endpoint information.

• Ensure quality standards, productivity, and delivery standards per project requirements.

• Comply with all project-related processes and activities.

• Create, maintain, and track cases as per the project plan.

• Liaise with different functional team members and health care professionals to address project-related issues.

• Lead/Support department Initiatives and ensure 100% compliance towards all people practices and processes.

Qualifications

• High School Diploma or equivalent in Scientific or healthcare discipline or allied life sciences.

• Bachelor’s degree in life sciences or related field and up to 3 years of relevant experience, inclusive of up to 1 year of Pharmacovigilance experience.

• Good knowledge of medical terminology.

• Working knowledge of applicable Safety Database and any other internal/Client applications.

• Strong verbal/written communication skills.

#LI-JM #LI-REMOTE

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 https://jobs.iqvia.com