Associate Director, Regulatory Medical Writing, Oncology

Johnson & Johnson

Allschwil, Switzerland
Base: $137,000 to $235,750; bonus/equity: eligible...
Fully remote
Regulatory medical writing experience
Clinical regulatory documents
Process improvement initiatives
Johnson & Johnson is seeking an Associate Director for Regulatory Medical Writing in Oncology, focusing on innovative treatments and patient-centered solutions. The role requires extensive experience in medical writing and project management, with responsibilities including leading writing teams and ensuring compliance with regulatory standards

Job Summary

  • Lead in setting functional tactics/strategy and project-level strategy, representing the therapeutic area head at high-level meetings with independent decision-making authority.
  • Responsible for writing and coordinating complex clinical and regulatory documents, establishing and driving document timelines and strategies, and guiding/training cross-functional team members.
  • Eligible for annual performance bonus, medical, dental, vision, life insurance, disability, retirement plan, savings plan, and long-term incentive program.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking an Associate Director for Regulatory Medical Writing in Oncology, focusing on innovative treatments and patient-centered solutions. The role requires extensive experience in medical writing and project management, with responsibilities including leading writing teams and ensuring compliance with regulatory standards.

Salary

Base: $137,000 to $235,750; Bonus/Equity: Eligible for annual performance bonus and long-term incentive program; Benefits: Medical, dental, vision, life insurance, disability, retirement plan, savings plan, time off benefits

Skills & Requirements

Must-have

  • Regulatory medical writing experience
  • Clinical regulatory documents
  • Process improvement initiatives
  • Cross-functional collaboration
  • People management experience

Nice-to-have

  • Championing internal standards
  • Leading by example
  • Acting as change agent
  • Mentoring junior staff
  • Interpreting statistical and medical information

Key Requirements

  • Minimum of a Bachelor's Degree
  • Minimum of 10 years pharmaceutical/scientific experience
  • Minimum of 8 years clinical/regulatory medical writing experience
  • Minimum of 2 years people management experience

Work Rights

Not specified

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