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 practices
Requirements:
• Degree in Life Sciences; 5 years’ industry experience
• Proven leadership in cross-functional project delivery
• Familiarity with drug/device regulations and documentation
• Expertise in clinical safety and regulatory writing
Drive impactful regulatory strategies and contribute your medical writing expertise within Client’s innovative setting.
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📌 Senior Medical Writer in Mississauga
🏢 US Tech Solutions
📍 Mississauga