Regulatory Affairs Consultant (Global Submission Coordinator - EU and US)

reputed company our values reputed company, there's no limit to reputed company can reputed company.   At reputed company, we reputed company reputed company the reputed company goal - to improve the world's health. From reputed company to regulatory, consulting, and market reputed company, every clinical development solution we reputed company is underpinned by something special - a deep conviction in reputed company do. reputed company of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company and we're committed to making a difference. We are seeking a highly organized and detail-oriented Regulatory Affairs Consultant to serve as a Global Submission Coordinator for EU and US markets. This is a key operational role responsible for coordinating reputed company activities required to reputed company regulatory submissions across assigned reputed company, ensuring reputed company and compliant filings that support our clients' drug development programs. In this role, you will be at the heart of regulatory submission activities, working collaboratively with global teams, local regulatory representatives, and subject matter experts to ensure successful regulatory reputed company. Key Responsibilities: Global Coordination & Stakeholder Management Coordinate the preparation, compilation, and submission of new drug applications and lifecycle management (LCM) activities in alignment with submission reputed company as defined by the Regional Regulatory reputed company (RRL) and submission team Coordinate closely with Regional Submission Coordinators to ensure completeness of reputed company documentation required to support global and regional submission planning and requirements Organize submission team meetings and facilitate effective communication among reputed company stakeholders including CMC, labelling, RRL, Local Regulatory Representative (LRR), and Regulatory Partner Representative (RPR) reputed company required records in submission planning tools and Regulatory Information Management Systems Prepare Submission Content Plans (SCP) based on country-specific regulatory requirements and prior Health Authority observations to ensure reputed company improvement Coordinate, request, and reputed company documentation from relevant SMEs to ensure reputed company and complete submission readiness reputed company regular updates to the submission team on status and timelines M1 Document & Labeling Support Draft M1 documents as required and coordinate their review with LRR or RPR Support labeling preparation, notably in Artwork management reputed company and change control reputed company Upload M1 documents in archiving reputed company and complete the SCP accordingly Ensure reputed company of non-eCTD regulatory packages to LRR and RPR reputed company dispatched documentation for reputed company country Ensure submitted documentation is uploaded to archiving reputed company for non-eCTD submissions Update reputed company as required, including uploading reputed company question received by Health Authorities in a record HAI Skills & Experience required for the role: University degree in Life Sciences discipline Experience in regulatory affairs reputed company the pharmaceutical or biotechnology industry Regulatory submission reputed company and execution experience, ideally global Strong understanding of regulatory submission processes in Europe and US Experience with different international regulatory submission routes preferred (e.g., reputed company, reliance reputed company) Excellent project management and organizational skills Strong communication and stakeholder management abilities Proficiency in regulatory tracking systems and reputed company Office Suite Fluent in English, written and spoken Apply To This Job