Associate Director, Regulatory Medical Writing, Oncology

Johnson & Johnson MedTech

Toronto, Ontario, Canada
Base: $162,750 - $212,750 cad; bonus/equity: discr...
Fully remote
Regulatory medical writing expertise
Project and process management
Cross-functional team leadership
Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases with a focus on patient-centered advancements

Job Summary

  • Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases with a focus on patient-centered advancements.
  • The Associate Director will lead medical writing teams, manage complex regulatory documents, and contribute to cross-functional strategy and process improvements.
  • This role offers opportunities to influence internal standards, mentor staff, and collaborate with senior colleagues and external partners to drive oncology treatment development.

Matching Summary

Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases with a focus on patient-centered advancements.

Salary

Base: $162,750 - $212,750 CAD; Bonus/Equity: Discretionary performance bonus eligible; Benefits: Not specified

Skills & Requirements

Must-have

  • Regulatory medical writing expertise
  • Project and process management
  • Cross-functional team leadership
  • Clinical and regulatory document coordination
  • Medical writing team management
  • Knowledge of ICH regulatory guidelines
  • Stakeholder communication and collaboration

Nice-to-have

  • Coaching and mentoring junior writers
  • Change management and adaptability
  • Strong leadership and negotiation skills
  • Ability to act as change agent
  • Expert time management
  • Inclusive leadership
  • Process improvement initiatives

Key Requirements

  • Minimum 10 years pharmaceutical/scientific experience
  • Minimum 8 years clinical/regulatory medical writing experience
  • Minimum 2 years people management experience
  • Bachelor's degree required; advanced degree preferred
  • Experience with ICH regulatory guidance
  • Project management and process improvement experience

Work Rights

Not specified

Tailored Resume

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