Senior Manager, Regulatory Strategy
- Lead the preparation, submission, management and maintenance global regulatory submissions including IND / CTAs, amendments, information requests, Orphan Drug Applications, DSUR / IB, and Marketing Applications etc.
- Coordinate and prepare for Agency meetings and meeting package preparation.
- Provide strategic regulatory input on clinical development plans, CMC strategies, and nonclinical programs to support regulatory milestones.
- Contribute to regulatory intelligence and interpretation of evolving global regulatory requirements, guidances, and precedents.
- Manage regulatory queries and commitments, works with experts on responses, and provides regular status updates.
- Identifies regulatory risks and creates mitigation plans.
- Develop and draft regulatory strategy components, analyses, and position statements.
- Interpret health authority feedback and propose recommended paths forward for internal discussion.
- Provide routine regulatory guidance to cross-functional teams on applicable regulations, guidances, and precedents.
- Manage day-to-day regulatory activities and timelines for assigned deliverables.
- Bachelor's degree in life sciences or related field.
- Advanced degree (doctorate or masters) is preferred.
- At least 2 years in regulatory strategy.
- Ex-US regulatory submission experience.
- Understanding of global regulatory frameworks (FDA, EMA, ICH).
- Excellent written and verbal communication skills.
- Advanced proficiency with Word.
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