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 programsServe as the key regulatory liaison with Health CanadaOversee submission quality and regulatory documentationProvide insights for clinical trial and labelling strategiesManage vendor relationships for high-quality regulatory submissionsRequirements:Degree in biological sciences or related field, advanced degree preferred12+ years of regulatory experience, especially in oncologyProficient in navigating Canadian regulatory landscapesExcellent organizational and leadership capabilitiesBilingual in English and French is an assetPosition yourself as a key leader in regulatory affairs and drive oncology success in Canada.#J-18808-Ljbffr

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