Manager, Regulatory Policy & Intelligence

At Insmed, every moment and every patient counts — and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you’ll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person’s contributions to meaningful progress. That commitment has earned us recognition as Science magazine’s No. 1 Top Employer for five consecutive years, certification as a Great Place to Work® in the U.S., and a place on The Sunday Times Best Places to Work list in the UK. For patients, for each other, and for the future of science, we’re in. Are you? About the Role: We're looking for a Manager, Regulatory Policy & Intelligence, on the Regulatory Affairs team to help us expand what’s possible for patients with serious diseases. Reporting to the Senior Director, Regulatory Affairs Strategist, you will serve as a critical resource for global regulatory intelligence - monitoring the evolving regulatory landscape, managing complex policy projects, and ensuring key stakeholders across Insmed are equipped with the regulatory insights needed to make sound, strategic decisions. What You'll Do: Monitor global regulatory intelligence across major Health Authorities, identifying emerging trends and developments that impact Insmed's current and future programs and strategic business objectives. Source and synthesize key regulatory documents - including guidance documents, policies, and regulations - to support the subunit's strategic assessment of significant regulatory topics. Anticipate and track regulatory changes over time, delivering timely, accurate, and actionable updates to impacted stakeholders across the organization. Lead cross-functional policy projects as project manager, driving alignment, accountability, and the delivery of high-quality outputs that reflect the perspectives of all relevant stakeholders. Champion continuous improvement within the subunit, proactively identifying opportunities to enhance processes, tools, and ways of working. Communicate with clarity and transparency, ensuring stakeholders remain informed, prepared, and confident in the face of a dynamic global regulatory environment. Who You Are: You have a Bachelor’s degree in a relevant scientific field along with 5 years of pharmaceutical industry experience.  You are or you also have: Detail-oriented and actively pursue knowledge beyond immediate scope of expertise, demonstrating sound judgement in ambiguous situations and taking full ownership of work from initiation through completion Managing multiple priorities simultaneously without compromising quality and recalibrating effectively when circumstances or priorities shift Embracing a continuous improvement mindset – any process can be refined to better serve its objective and pursuing that change is both necessary and worthwhile Cultivating genuine, trust-based relationships across functions and levels of the organization Approaching challenges with confidence and optimism Nice to have (but not required): Background in Regulatory Affairs Project management experience with cross-functional teams Where You’ll Work This is a fully remote role. It can be performed effectively from anywhere while staying connected to your Insmed team and community. Occasional travel for team meetings or events will be expected. Travel Requirements This role requires occasional domestic and international travel (approximately 5%–15%) #LI-JK #LI-Remote Pay Range: $133,000.00-173,000.00 Annual Life at Insmed At Insmed, you’ll find a culture as human as our mission—intentionally designed for the people behind it. You deserve a workplace that reflects the same care you bring to your work each day, with support for how you work, how you grow, and how you show up for patients, your team, and yourself. Highlights of our U.S. offerings include: Comprehensive medical, dental, and visio ... (truncated, view full listing at source)