Pharmacovigilance Regulatory Reporting, Trilingual

🔥 6 minutes ago

🌐 United States, Brazil, +1 more countries – Remote

🇺🇸 United States – Remote 🇧🇷 Brazil – Remote 🇦🇷 Argentina – Remote

⏰ Full Time

🟢 Junior

🚔 Compliance

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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IQVIA

WebsiteLinkedInAll Job Openings

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

• Submit safety reports to regulatory authorities • Review, assess, and process safety data and information from various sources • Distribute reports/data to internal and external third parties according to applicable regulations, SOPs, and internal guidelines • Process safety data according to regulations, guidelines, SOPs, and project requirements • Ensure compliance with quality, productivity, and delivery standards • Track cases according to the project plan • Identify and report quality problems to senior team members • Liaise with functional team members and healthcare professionals on project-related issues • Attend project team meetings and provide feedback to the operations manager

🎯 Requirements

• Bachelor's degree in life sciences • Advanced level of English, Spanish and Portuguese • 1 year of experience in pharmacovigilance activities (mandatory) • Experience specifically in regulatory reporting highly valued • Previous experience working with Argus desirable • Good knowledge of medical terminology and applicable safety databases • Strong organizational skills and attention to detail • Ability to work independently and as part of a team

🏖️ Benefits

• 100% home-based work modality