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

microsatsystems.biz

Hybrid
10 years experience in regulatory affairs
Strong communication and time management skills
Experience with health canada submissions
The Associate Director of Regulatory Affairs in Clinical Oncology will oversee clinical specialists and manage regulatory projects for oncology products. This hybrid role requires extensive experience in regulatory affairs, particularly in oncology, along with strong communication and collaboration skills

Job Summary

  • The Associate Director will lead regulatory projects within the oncology portfolio.
  • This role involves oversight of key regulatory submissions and collaboration with various stakeholders.
  • The company values diversity and encourages an inclusive work environment.

Matching Summary

Match Score: 85

The Associate Director of Regulatory Affairs in Clinical Oncology will oversee clinical specialists and manage regulatory projects for oncology products. This hybrid role requires extensive experience in regulatory affairs, particularly in oncology, along with strong communication and collaboration skills.

Skills & Requirements

Must-have

  • 10 years experience in regulatory affairs
  • Strong communication and time management skills
  • Experience with Health Canada submissions

Nice-to-have

  • Ability to work independently
  • Strong collaboration and teamwork skills
  • Visible commitment to service and company

Key Requirements

  • Advanced University Degree in Health Sciences
  • Oncology expertise preferred
  • Fluency in French required

Work Rights

Not specified

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