Advance your career as a Senior Medical Writer at Client’s Mississauga campus. This onsite role focuses on regulatory data interpretation and content strategy for clinical projects.As a key member of the Pharma Development Regulatory organization, you will manage teams to ensure the delivery of high-quality regulatory submissions. Your expertise in medical writing and collaborative skills will support strategic initiatives in drug and device development, guaranteeing compliance with industry standards and regulations.Key Responsibilities:- Lead cross-functional teams for regulatory content development- Create timelines for document production and reviews- Review documents for quality, clarity, and compliance- Resolve issues with contributors and ensure adherence to regulations- Mentor junior Content Strategists on best practicesRequirements:- Degree in Life Sciences; 5 years’ industryexperience- Proven leadership in cross-functional project delivery- Familiarity with drug/device regulations and documentation- Expertise in clinical safety and regulatory writingDrive impactful regulatory strategies and contribute your medical writing expertise within Client’s innovative setting.#J-18808-Ljbffr

📌 Associate Medical Writer - C$115,000 - C$130,000 A Year (Winnipeg)
🏢 Amaris Consulting
📍 Winnipeg