The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes
Job Summary
The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes.
Collaboration with internal and external stakeholders is essential to maintain high quality and timely execution of the processes.
Supporting simplification and optimization of case management activities to enhance overall effectiveness.
Matching Summary
The Safety Data Lead is responsible for the analysis and interpretation of adverse experience (AE) reports of varying complexity, in compliance with regulatory requirements and internal processes.
Skills & Requirements
Must-have
Adverse experience report analysis
Regulatory compliance
Case management activities
Pharmacovigilance
Clinical data cleaning
Nice-to-have
Business savviness
Networking and partnerships
Strategic planning
Motivation and inspiration
Learning agility
Key Requirements
Bachelor’s degree or above in health care or life sciences
Advanced writing/reading and intermediate speaking/listening English
Understanding of pharmacovigilance-related regulations is desired