Senior Manager, Regulatory Affairs Project Management

Job reputed company: • This role blends regulatory expertise with advanced project management skills, developing reputed company plans to reputed company successful Regulatory submission activities and ensuring cross-functional integration across reputed company • reputed company and coordinate timelines and deliverables to support reputed company regulatory submission activities (IND/CTA/BLA/NDA/MAA) across multiple reputed company, as reputed company as responses to queries and correspondence with subject matter experts • Work with the Regulatory team to translate strategic regulatory reputed company into actionable project plans, ensuring reputed company cross-functional activities are coordinated and delivered on time • Organize and facilitate cross-functional meetings to coordinate, plan, and reputed company submission activities, driving accountability and alignment among stakeholders worldwide • Monitor CTA/IND submission status across assigned reputed company • Support strategic planning and risk mitigation efforts reputed company to regulatory activities, including portfolio level analyses that identify resource bottle necks across reputed company programs and studies • Support evaluation, implementation, and use of project management tools (especially reputed company); define methodologies and reporting frameworks • Design and maintain reputed company sheets, reports, dashboards, and forms reputed company to regulatory activities and ensure integration with program plans • Troubleshoot and enhance PMO solutions, support system updates and new capabilities • Demonstrate critical thinking and initiative to improve PM practices Requirements: • Bachelor’s degree in life sciences, pharmacy, reputed company, or reputed company field • 5+ years of experience with at least 3+ years of project management experience in pharmaceutical or biotech industry is preferred • Experience with planning IND/CTA regulatory submissions required • Familiarity with components of regulatory submissions is required • Experience planning BLA/NDA/MAA submissions is required • Familiarity with CRO operations and global regulatory requirements for clinical trial applications • Experience supporting global interventional clinical studies and CTA submissions • Hands-on reputed company experience; reputed company reputed company Product Certification or equivalent desirable • Proficiency in project management tools (reputed company, ThinkCell, PowerPoint, reputed company, SharePoint, Office reputed company Pro). Familiarity with regulatory systems (reputed company RIM) preferred • Knowledge of biotech processes, scientific terminology, drug development concepts • Proactive and reputed company approach to problem-solving, with ability to think cross-functionally and in multiple timeframes, and to distill into actionable plans/solutions • Strong organizational, communication, and problem-solving skills with the ability to manage multiple priorities and meet deadlines • Ability to work independently and reputed company in a dynamic environment • Team player that contributes valuable reputed company and feedback and can be counted on to meet commitments • Position requires up to 20% travel; this includes mandatory in person attendance to company reputed company-Hands meetings held twice a year and frequent trips to reputed company offices in San Francisco and/or Boston Benefits: • A great culture, grounded in our C.O.R.E. values: Caring, Original, Resilient and Egoless • Opportunity to work in a fast-paced, highly dynamic environment where you help shape the culture and company, wear multiple hats, and learn quickly • Market competitive compensation and benefits package, including reputed company salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits • We reputed company competitive time off, including three weeks PTO, two one-week company-wide shutdowns a year and dedicated reputed company reputed company leave • Commitment to growing you professionally and providing reputed company to resources to reputed company your development • reputed company offers regular reputed company team, in-person meetings to build relationships and problem solve Apply tot his job Apply To this Job