Directeur(rice) Associé(e), Affaires Réglementaires - Oncologie Clinique/ Associate Director, Regulatory Affairs - Clinical Oncology

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Health canada regulatory submissions
Oncology portfolio management
French language proficiency required
** The position of Associate Director in Regulatory Affairs for Clinical Oncology involves leading and supervising oncology regulatory projects, ensuring compliance with Health Canada regulations, and fostering a collaborative team environment. The ideal candidate should have at least 10 years of regulatory affairs experience, particularly in oncology, and must possess strong communication and leadership skills. **

Job Summary

  • The Associate Director leads regulatory projects within the oncology portfolio, including planning and assigning tasks to specialists.
  • This role serves as the primary contact for Health Canada regarding oncology product registrations, safety issues, and priority review requests.
  • The position requires a candidate with advanced communication skills to effectively engage with clinical, commercial, and government stakeholders.

Matching Summary

Match Score: 75

** The position of Associate Director in Regulatory Affairs for Clinical Oncology involves leading and supervising oncology regulatory projects, ensuring compliance with Health Canada regulations, and fostering a collaborative team environment. The ideal candidate should have at least 10 years of regulatory affairs experience, particularly in oncology, and must possess strong communication and leadership skills. **

Skills & Requirements

Must-have

  • Health Canada regulatory submissions
  • Oncology portfolio management
  • French language proficiency required
  • Food and Drug Act knowledge
  • Clinical regulatory project leadership

Nice-to-have

  • Virtual team environment creation
  • Continuous process improvement focus
  • Cross-cultural collaboration skills
  • Strategic thinking in oncology
  • Change management initiatives

Key Requirements

  • Minimum 10 years experience in clinical regulatory affairs
  • M.Sc. or higher degree in Health Sciences
  • Completed New Drug Submission filings to Health Canada
  • Fluent in French (written and oral)
  • Demonstrated knowledge of Health Canada Food and Drug Act

Work Rights

Not specified

Tailored Resume

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