Associate Director, Safety Analysis Scientist

Johnson & Johnson

Raritan, New Jersey, United States of America
Base: $137,000 - $235,750; bonus/equity: eligible ...
Hybrid (3 days on-site)
Safety analysis and evaluations
Lead safety data review meetings
Product safety strategy
Johnson & Johnson is seeking an Associate Director, Safety Analysis Scientist, to lead safety evaluations and analysis for their Innovative Medicine division, particularly in oncology. This hybrid role requires strong expertise in medical writing, pharmacovigilance, and the ability to collaborate across teams to support safety management for various products

Job Summary

  • The Associate Director (AD) Safety Analysis Scientist (SAS) provides scientific expertise and leads the safety assessment of assigned products.
  • This is a hybrid position that requires you to be on site three days a week.
  • The anticipated base pay range for this position in the US is $137,000 to $235,750.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking an Associate Director, Safety Analysis Scientist, to lead safety evaluations and analysis for their Innovative Medicine division, particularly in oncology. This hybrid role requires strong expertise in medical writing, pharmacovigilance, and the ability to collaborate across teams to support safety management for various products.

Salary

Base: $137,000 - $235,750; Bonus/Equity: Eligible for annual performance bonus; Benefits: Medical, dental, vision, life insurance, disability, retirement plan, 401(k), vacation, sick time, holiday pay, personal time

Skills & Requirements

Must-have

  • Safety analysis and evaluations
  • Lead safety data review meetings
  • Product safety strategy
  • Health Authority interactions
  • Cross-functional training

Nice-to-have

  • Innovative approaches to data presentation
  • Independent influence and negotiation
  • Proactive safety data reviews
  • Act as product SME for audits

Key Requirements

  • Bachelor’s Degree in Healthcare-related or Biomedical Science
  • 11+ years industry experience or equivalent
  • Medical writing or Pharmacovigilance experience
  • Working knowledge of medical concepts
  • Ability to understand and analyze complex medical-scientific data
  • Excellent English verbal and written communication skills

Work Rights

Not specified

Tailored Resume

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