The Associate Director of Regulatory Affairs is responsible for the management of regulatory affairs activities including pharmacovigilance work at the RA department
Job Summary
The Associate Director of Regulatory Affairs is responsible for the management of regulatory affairs activities including pharmacovigilance work at the RA department.
The individual will ensure that the RA team develops and successfully executes project plans for timely product registrations and will motivate and encourage the RA Team to perform successfully.
The position requires a combination of scientific knowledge, understanding of regulatory requirements, strategic thinking, and team leadership to ensure timely development of new products and regulatory affairs activities.
Matching Summary
The Associate Director of Regulatory Affairs is responsible for the management of regulatory affairs activities including pharmacovigilance work at the RA department.
Skills & Requirements
Must-have
Regulatory Affairs
Pharmacovigilance
Product Registrations
Team Leadership
Scientific Knowledge
Regulatory Requirements
Nice-to-have
Cross-Team Coordination
Strategic Thinking
Empowering Leadership
Future-Oriented
Innovative Mindset
Key Requirements
Minimum 7 years of relevant experience
Veterinarian or PhD in Biological or Animal Sciences preferable
Experience leading teams
Knowledge of Japanese Regulatory System preferable