We are seeking a highly experienced and strategically driven Associate Director of Regulatory Affairs to lead and support the development and execution of global regulatory strategies across complex development programs. This role offers an excellent opportunity for a regulatory professional with strong European expertise and broad global exposure to contribute to the advancement of innovative medicinal products through all stages of development and registration.
The successful candidate will play a pivotal role in shaping and implementing regulatory strategies across multiple geographies, with a particular focus on Europe. Lead and support the development and execution of global regulatory strategies for development-stage and marketed products. Provide strategic input across key regulatory activities, including initial MAA, ODD, Scientific Advice, and PIPs, while acting as a primary interface with the EMA and other health authorities. Drive regulatory planning for major development milestones and market expansion, partnering cross-functionally to ensure aligned execution, effective risk management, and lifecycle optimization
Ensuring the primary contact to Competent Authorities within Europe and other regions as required
Identifying the need and obtaining regulatory intelligence, researching precedent approvals and prior health authority decisions to assess applicability to support development of strategic options for assigned Otsuka products
Translating complex pertinent global requirements and providing an assessment of the associated regulatory challenges to the GRL, global regulatory team, assigned project teams, and internal/external functional business units as needed
Leading a cross functional team to collaboratively develop a global regulatory plan, address global regulatory issues, respond to health authority queries, and meet regulatory obligations including a focus on European requirements as needed per responsibility
Developping and leading strategy for Health Authority interactions/communications through submissions and responding to regulatory authorities within company timelines and in accordance with regulations and guidelines
Reviewing submission documents to ensure they are aligned with the strategic approach developed by the cross functional team
Designing programs for complete and accurate IND/CTA/NDA/MAA and other submissions and ensuring that clinical trials are designed to meet regulatory requirements
Supporting development of strategies, drafts responses, and/or reviewing responses and documents intended for submission to health authorities to assure compliance with regulatory standards
Reviewing submission documents for consistency and ensuring they are aligned with strategic approach developed by the team
Interacting with regulatory agencies and ensuring conversations and communications are focused, amicable and documented
Contributing to the submission of product registration of new drugs, progress reports, supplements, amendments, aggregate reports and periodic adverse experience reports
Collaborating and providing oversight to outsourced suppliers of regulatory support in the preparation of documents/reports
Identifying early major regulatory issues and ensures these are communicated to relevant stakeholders in a timely manner
