Pharmacovigilance Regulatory Reporting (Trilingual)

Experteer Overview In this role you will process safety data to support regulatory submissions and ensure compliance with SOPs and project requirements. You will coordinate reporting of safety information to regulatory authorities and internal/external partners, under guidance from senior team members. You will work across functions and healthcare professionals to address project challenges, attending meetings and providing feedback. The position is fully remote, leveraging multilingual capabilities to support pharmacovigilance activities in English, Spanish, and Portuguese. This role offers a meaningful impact on patient safety and regulatory compliance within a global team.

Compensaciones / Beneficios

• Process safety data per regulations, guidelines, SOPs, and project needs
• Ensure quality, productivity, and on-time delivery per project requirements
• Track cases aligned with the project plan
• Identify and report quality problems to senior team members
• Liaise with cross-functional teams and healthcare professionals to resolve issues
• Attend project team meetings and provide feedback to operations management

Responsabilidades

• Bachelor's degree in life sciences
• Languages: Advanced English, Spanish, and Portuguese
• 1 year of pharmacovigilance experience, specifically regulatory reporting
• Experience with Argus is desirable
• Strong medical terminology knowledge and safety databases
• Excellent organizational skills, attention to detail, ability to work independently and in a team

Requisitos principales

• 100% home-based
• remote work
• flexible work arrangement
• collaborative tools

Pharmacovigilance Regulatory Reporting (Trilingual)

Madrid, ES