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

Vetamc

Hybrid
10 years of regulatory affairs experience
Strong communication and time management skills
Knowledge of health canada regulations
The position of Associate Director, Regulatory Affairs for Clinical Oncology at Vetamc involves overseeing regulatory projects related to oncology products, ensuring compliance with Health Canada, and leading a team of clinical specialists. The ideal candidate should possess significant experience in regulatory affairs, especially in oncology, along with strong communication and collaboration skills

Job Summary

  • The Associate Director will oversee regulatory projects in oncology and manage a team of specialists.
  • This role requires a deep understanding of product registrations and regulatory submissions.
  • The company values diversity and encourages a collaborative work environment.

Matching Summary

Match Score: 85

The position of Associate Director, Regulatory Affairs for Clinical Oncology at Vetamc involves overseeing regulatory projects related to oncology products, ensuring compliance with Health Canada, and leading a team of clinical specialists. The ideal candidate should possess significant experience in regulatory affairs, especially in oncology, along with strong communication and collaboration skills.

Skills & Requirements

Must-have

  • 10 years of regulatory affairs experience
  • Strong communication and time management skills
  • Knowledge of Health Canada regulations

Nice-to-have

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

Key Requirements

  • Advanced University Degree in Health Sciences
  • Experience with New Drug Submission filings
  • Fluency in French required

Work Rights

Not specified

Tailored Resume

Cover Letter