International Program Regulatory Associate Director (iprad)
Novartis
Hyderabad, India
On-site
Registration strategies and plans
Pipeline planning
Country requirements maintenance
The International Program Regulatory Associate Director supports the design and execution of optimal registration strategies and plans for assigned portfolios in International countries
Job Summary
The International Program Regulatory Associate Director supports the design and execution of optimal registration strategies and plans for assigned portfolios in International countries.
This role involves partnering with stakeholders to optimize pipeline planning, account for regional priorities, and ensure efficient use of regulatory paths for acceleration.
Key responsibilities include driving the execution of registration plans, maintaining country requirement databases, and supporting initiatives to enhance efficiency in ways of working.
Matching Summary
The International Program Regulatory Associate Director supports the design and execution of optimal registration strategies and plans for assigned portfolios in International countries.
Skills & Requirements
Must-have
registration strategies and plans
pipeline planning
country requirements maintenance
cross-functional collaboration
HA negotiations
project management expertise
Nice-to-have
functional excellence initiatives
matrix leadership skills
organizational awareness
team oriented
Key Requirements
Minimum of 8 years in Regulatory or product development
Minimum of 1 year country, regional or global Regulatory experience