Drive the regulatory strategy, planning and execution across key regions for the assigned development pipeline projects (from early pre-clinical phases)
Collaborate with cross-functional teams to ensure timely submissions, approvals, and compliance with global regulatory requirements, supporting the successful development and registration of innovative pharmaceutical products.
Major Activities Key Responsibilities Develop and implement Global regulatory strategies for assigned pipeline development programs, ensuring alignment with global regulatory requirements and company objectives.
Provide regulatory input into R&D; programs to ensure they meet regulatory expectations
Prepare, review, and manage regulatory submissions including INDs, NDAs, MAAs, ensuring accuracy, completeness, and timely delivery.
Coordinate responses to health authority queries, ensuring scientifically sound and compliant answers within required timelines.
Monitor evolving regulatory requirements across major markets (FDA, EMA, ICH,)

and proactively assess their impact on development programs and submission strategies.
Collaborate with cross-functional teams (R&D;, Clinical Development, CMC, Safety, Quality, business etc ) to ensure integrated regulatory plans
Support regulatory meetings and interactions with health authorities, including briefing document preparation
Ensure compliance with internal SOPs and global standards, contributing to continuous improvement initiatives and best practices in regulatory operations.
Review and approve Clinical Trials Applications (CTAs)
Perform regulatory Due Diligence activities for acquisition of new assets in development stages to enhance Company pipeline
Job Dimensions Ideal Background Degree in a scientific field
Languages: Fluent in written and spoken English
Experience/Professional requirement: More than 5 years of successful managerial experience in the pharmaceutical industry with a proven track record of successful registrations of innovative produc

Global Program Regulatory

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