Elevate your career with Fusion Pharmaceuticals as a CMC Regulatory Affairs Lead. This role involves managing regulatory submissions, ensuring compliance across programs while collaborating with cross-functional stakeholders.As a pivotal member of the CMC team, you will execute and coordinate regulatory activities for innovative oncology programs. This position demands expertise in regulatory systems and document management, with a focus on high-quality submission deadlines. Strong organizational skills and keen attention to detail are essential for this hands-on role.Key Responsibilities:
- Coordinate CMC regulatory submission activities across multiple programs
- Author and develop complex regulatory documents clearly
- Track document development and ensure submission readiness




- Maintain CMC regulatory submission trackers and timelines
- Support responses to health authority inquiriesRequirements:
- Bachelor’s degree in a scientific or regulatory discipline
- Experience in CMC regulatory affairs, preferably in pharmaceuticals
- Solid understanding of regulatory submission processes
- Exceptional organizational and project coordination skills
- Ability to manage multiple concurrent deliverablesBe the driving force behind regulatory excellence at Fusion Pharmaceuticals, ensuring all submissions are timely and compliant.#J-18808-Ljbffr

📌 Cmc Regulatory Affairs Lead At Fusion Pharmaceuticals (Hamilton)
🏢 AstraZeneca
📍 Hamilton