Elevate your career at Alexion as a Lead Medical Writer responsible for high-quality clinical documents. This 6-month contract emphasizes regulatory submissions and scientific clarity within a versatile work environment.As an Associate Director of Medical Writing, you will drive medical writing efforts across diverse clinical programs. Your expertise will be crucial in authoring protocols, study reports, and regulatory submissions. By translating complex data into clear narratives, you contribute to groundbreaking medicines that change lives.Key Responsibilities:Author clinical documents including protocols and reportsDevelop briefing packages for health authority inquiriesSupport clinical teams by delivering high-quality documentsNegotiate timelines across functionsMentor junior medical writers and ensure adherence to standardsRequirements:Experience in clinical regulatory writing and submissionsProficiency in writing investigational documentsStrong knowledge of global regulatory and ICH standardsExcellent project management and negotiation skillsAdvanced proficiency in MS Office suiteYour skills in medical writing and regulatory understanding will significantly impact patient solutions at Alexion.#J-18808-Ljbffr

📌 Lead Medical Writer At Alexion (Mississauga)
🏢 Alexion Pharmaceuticals,Inc.
📍 Mississauga