Advance your career as a Senior Director of Regulatory Affairs in Canada with a leading biopharmaceutical company. Spearhead regulatory strategies in oncology and ensure compliance across all processes. As the head of Regulatory Affairs, you will report to the Vice-President & General Manager, providing strategic guidance and regulatory expertise.

You’ll be responsible for overseeing the entire product lifecycle, ensuring that Canadian regulatory frameworks are seamlessly integrated into global strategies. Your proactive leadership will be essential for successful external collaborations. Key Responsibilities:
Develop comprehensive regulatory strategies for oncology programs
Serve as the key regulatory liaison with Health Canada




Oversee submission quality and regulatory documentation
Provide insights for clinical trial and labelling strategies
Manage vendor relationships for high-quality regulatory submissions Requirements:
Degree in biological sciences or related field, advanced degree preferred
12+ years of regulatory experience, especially in oncology
Proficient in navigating Canadian regulatory landscapes
Excellent organizational and leadership capabilities
Bilingual in English and French is an asset Position yourself as a key leader in regulatory affairs and drive oncology success in Canada.

📌 Senior Director, Regulatory Affairs Role Toronto
🏢 MedAccess Recruiters
📍 Toronto