About me
Samir Ledade is an Associate Director, Medical Writing Operations at Alexion Pharmaceuticals, based in Mississauga, Canada. He has over 16 years of experience in regulatory medical writing, clinical development, and pharmacovigilance within global pharmaceutical organizations. His primary area of work has been in oncology, where he has authored and overseen a wide range of clinical and safety documents across Phase I–IV programs. Samir has supported regulatory submission activities and contributed to vendor/resource management, inspection readiness initiatives, and the implementation of innovative medical writing technologies and standards. Prior to Alexion, he held progressive leadership and SME roles supporting global regulatory programs.
