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.
#J-18808-Ljbffr

📌 Senior Director, Regulatory Affairs Role (Ontario)
🏢 MedAccess Recruiters
📍 Ontario