IQVIA
10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
Pharmacovigilance Regulatory Reporting, Trilingual
🔥 3 minutes ago
🗣️🇪🇸 Spanish Required
🗣️🇧🇷🇵🇹 Portuguese Required
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IQVIA
10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
📋 Description
• Involved in submitting safety reports to regulatory authorities • Review, assess, and process safety data and information received from various sources • Distribute reports/data to internal and external third parties following applicable regulations, SOPs, and internal guidelines • Track cases as applicable to the project plan • Identify and report quality problems to senior team members • Liaise with different functional team members and health care professionals to address project-related issues • Attend project team meetings and provide feedback to the operations manager on challenges, issues, or successes
🎯 Requirements
• Bachelor's degree in life sciences • Advanced level of English, Spanish and Portuguese • 1 year of experience in pharmacovigilance activities (mandatory) • Previous experience working with Argus is desirable • Good knowledge of medical terminology and applicable safety databases • Strong organizational skills, attention to detail, and ability to work independently and as part of a team
🏖️ Benefits
• Home office setup allowance • Work modality: 100% home-based
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