Safety & PV Specialist

📋 Description

• ICSR Processing: enter and track safety information in pharmacovigilance quality and tracking
• Case Assessment & Data Quality: triage ICSRs and evaluate case information for completeness
• Medical Coding: code adverse events, medical history, concomitant medications, tests, and other
• Case Narratives & Follow-Up: prepare complete and accurate narrative summaries, identify
• Regulatory Reporting: support the timely, consistent, and accurate generation and submission of
• Literature & Safety Surveillance: perform literature screening and review activities related to

🎯 Requirements

• Education: Bachelor’s degree in a life-science discipline, or qualification as a registered nurse
• Pharmacovigilance Knowledge: practical knowledge of safety database systems and medical
• Clinical & Regulatory Understanding: good understanding of clinical trial processes across
• Technical Skills: proficiency with Microsoft Office Suite, including Word, Excel, and PowerPoint
• Analytical Skills: strong attention to detail, accuracy, and ability to identify inconsistencies or
• Organization: strong organizational and prioritization skills, with the ability to manage multiple

🎁 Benefits

• Remote Work: fully remote opportunity within Brazil, under the applicable pre-approved remote work
• Professional Development: opportunities for career development and progression within a global
• Training: access to technical and therapeutic-area training to strengthen pharmacovigilance and
• Supportive Management: engaged line management and collaboration with experienced professionals
• Recognition & Rewards: access to peer recognition initiatives and a total rewards program
• Global Collaboration: opportunity to work with multidisciplinary teams and international