
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.
🔥 15 hours ago
🗣️🇪🇸 Spanish Required
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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.
• Review, assess, and process safety data and information across service lines from various sources • Distribute reports/data to internal and external third parties following applicable regulations, SOPs, and internal guidelines • Process safety data according to applicable regulations, guidelines, SOPs, and project requirements • Perform pharmacovigilance activities, including collecting and tracking incoming Adverse Events (AEs) and endpoint information • Determine initial/update status of incoming events • Enter data into databases and code AEs and products • Write narratives and perform literature-related activities • Ensure compliance with quality, productivity, and delivery standards per project requirements • Liaise with functional team members and healthcare professionals to address project-related issues
• Bachelor's degree in Life sciences or a related field (mandatory) • Fluency in English and Spanish (mandatory) (will be evaluated) • 1 or 2 years of pharmacovigilance experience will be highly valued (desirable) • Experience with Safety Databases will be highly valued (ARGUS or others) (desirable)
• 100% home-based work modality
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