Job Description
Incredible opportunity to shape global regulatory strategy and deliver breakthrough science while working from home! We’re looking for a seasoned Regulatory Project Manager who can turn strategy into action and thrive in fast-moving, innovative environments. In this high-impact role, you’ll partner closely with Global Regulatory Leads to drive globally aligned regulatory plans, guide complex development and registration programs, and keep cross‑functional teams focused on what matters most. You won’t just manage timelines—you’ll enable clarity, anticipate risk, elevate team performance, and help bring transformative mRNA medicines to patients around the world. If you’re energized by complexity, motivated by impact, and inspired by the chance to help bring groundbreaking therapies to patients, this is your opportunity to make a meaningful difference. This role is designed for an experienced and forward-thinking regulatory project manager who thrives in a fast-paced, innovative environment and can seamlessly integrate strategic thinking with operational execution across all stages of product development, registration, and post-marketing. As a key member of the Global Regulatory Science team, you will partner strategically with Global Regulatory Leads to shape and execute comprehensive regulatory strategies for the U.S. and ex-U.S. markets. You will lead the development and execution of proactive global regulatory plans that articulate clear milestones, surface risks and opportunities, and support timely, informed regulatory decision-making. This is a highly visible, cross-functional role requiring strong leadership, agility, and strategic foresight. You will be accountable for driving regulatory excellence by aligning cross-functional stakeholders, managing complex timelines, and anticipating challenges to enable successful delivery of regulatory milestones that support sponsor’s mission to bring transforma