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

vetshired.us

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10 years experience in regulatory affairs
Strong communication skills
Knowledge of health canada regulations
** The Associate Director of Regulatory Affairs in Clinical Oncology is responsible for overseeing regulatory projects, managing submissions, and fostering collaboration within the oncology portfolio. Candidates should have a strong background in regulatory affairs, particularly in oncology, and must be fluent in French. **

Job Summary

  • The Associate Director is responsible for engaging and supervising Clinical Specialists on oncology projects.
  • This role includes oversight of regulatory submissions and maintaining compliance with Health Canada.
  • The company values diversity and encourages a collaborative work environment.

Matching Summary

Match Score: 75

** The Associate Director of Regulatory Affairs in Clinical Oncology is responsible for overseeing regulatory projects, managing submissions, and fostering collaboration within the oncology portfolio. Candidates should have a strong background in regulatory affairs, particularly in oncology, and must be fluent in French. **

Skills & Requirements

Must-have

  • 10 years experience in regulatory affairs
  • Strong communication skills
  • Knowledge of Health Canada regulations

Nice-to-have

  • Collaboration and teamwork skills
  • Commitment to ethical standards
  • Ability to work independently

Key Requirements

  • Advanced University Degree in Health Sciences
  • Experience with new product submissions to Health Canada

Work Rights

Not specified

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