Pharmacovigilance Specialist

About the role

The Pharmacovigilance Specialist will support the safety monitoring of medical products by reviewing, assessing, and processing safety data from multiple sources. Working remotely, you will ensure that all safety information is handled in compliance with regulations, SOPs, and internal guidelines.

Key responsibilities

• Process safety data according to applicable regulations, guidelines, SOPs, and project requirements.
• Collect, track, and assess incoming Adverse Events (AEs) and related endpoint information.
• Enter data into safety databases, code AEs and products, and draft narrative summaries.
• Perform literature‑related activities to support safety assessments.
• Maintain quality, productivity, and delivery standards as defined by the project.
• Collaborate with functional team members and healthcare professionals to resolve project‑related issues.

Required profile

• Bachelor’s degree in Life Sciences or a related field.
• Fluency in English and Spanish.
• Up to 3 years of clinical experience (preferred).
• At least 1 year of pharmacovigilance experience (highly valued).

Required skills

• Pharmacovigilance data processing.
• Adverse Event (AE) coding and database entry.
• Narrative writing for safety reports.

What we offer

• Annual performance‑based bonus.
• Salary adjustments aligned with inflation rates.
• 21 vacation days per year.
• 100% remote work arrangement.