Associate Director, Safety Scientist

📋 Description

• Lead safety signal identification and assessment across data sources.
• Develop data acquisition and analytical strategies for safety evaluations.
• Analyze safety data and write comprehensive safety reports.
• Collaborate with cross-functional scientists and physicians on safety assessments.
• Prepare safety data for governance bodies and safety committees.
• Facilitate safety team meetings and communicate with stakeholders.

🎯 Requirements

• PharmD/PhD in medical/biological sciences with 4+ years in analytical pharmacovigilance.
• RN with 8+ years in analytical pharmacovigilance; MD with clinical training also acceptable.
• Physician candidates with 2+ years in relevant safety science preferred.
• Strong pharmacovigilance knowledge, signal detection, risk management.
• Proven ability to analyze data and provide scientific recommendations.
• Knowledge of regulations (ICH), MedDRA, and safety databases.

🎁 Benefits

• Fully remote opportunity from Brazil.
• Full-time in a global pharmacovigilance environment.
• Opportunity to contribute to Phase I–III safety science activities.
• High visibility in safety governance and regulatory activities.
• Collaboration with international Safety, Clinical Development, and Regulatory teams.
• Professional growth via exposure to complex safety assessments.