Senior Regulatory Affairs Consultant - Senior Regulatory Project Manager

When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Incredible opportunity to shape global regulatory strategy and deliver breakthrough science while working from home! We’re looking for a seasoned Senior 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 vaccines 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 transformative vaccines to patients worldwide. In close partnership with Global Regulatory Leads, you will also play a key role in facilitating Global Regulatory Subteam (GRST) meetings and subteam forums, ensuring effective meeting structure, clear agendas, documented decisions and actions, timely follow-up, and strong meeting hygiene consistent with project management best practices. This includes helping teams operate with clarity, accountability, and a high-performance mindset through disciplined planning, communication, and execution. Here’s What You’ll Do - Partner strategically with Global Regulatory Leads to shape and execute forward-looking, globally aligned regulatory plans across all stages of development and post-marketing. - Translate regulatory strategy into integrated, actionable plans with clear milestones, critical paths, risks, and opportunities to support effective planning and decision-making. - Lead the execution of regulatory plans, ensuring alignment between day-to-day operations and broader strategic objectives across global programs. - Identify and propose innovative regulatory pathways and planning scenarios that align with global regulatory expectations and business objectives. - Collaborate closely with cross-functional teams and senior leadership to drive clarity, alignment, and accountability for regulatory deliverables, timelines, and interdependencies. - Facilitate Global Regulatory Subteam (GRST) meetings and other routine and ad hoc project revie