Associate Director, Safety Analysis Scientist

Johnson & Johnson

Titusville, New Jersey, United States of America
Base: $137,000 to $235,750; bonus: eligible for an...
Hybrid
Medical writing or pharmacovigilance experience
10 years industry experience with bachelor's degree
Ability to analyze complex medical-scientific data
The Associate Director Safety Analysis Scientist provides scientific expertise and leads the safety assessment of assigned products for Johnson & Johnson Innovative Medicine

Job Summary

  • The Associate Director Safety Analysis Scientist provides scientific expertise and leads the safety assessment of assigned products for Johnson & Johnson Innovative Medicine.
  • This role requires leading proactive safety data reviews, collaborating with Medical Safety Officers, and supporting Health Authority interactions regarding safety and risk management.
  • Employees are eligible for a competitive base pay range of $137,000 to $235,750 along with comprehensive benefits including parental leave, retirement plans, and performance bonuses.

Matching Summary

The Associate Director Safety Analysis Scientist provides scientific expertise and leads the safety assessment of assigned products for Johnson & Johnson Innovative Medicine.

Salary

Base: $137,000 to $235,750; Bonus: Eligible for annual performance bonus; Benefits: Medical, dental, vision, 401(k), pension, and extensive time off

Skills & Requirements

Must-have

  • Medical writing or Pharmacovigilance experience
  • 10 years industry experience with Bachelor's degree
  • Ability to analyze complex medical-scientific data
  • Experience with global safety health authority requirements
  • Proficiency in Microsoft Word Excel PowerPoint

Nice-to-have

  • Clinical experience preferred
  • Leadership skills in matrix environment
  • Innovative approaches to data presentation
  • Cross-functional training capabilities
  • Subject Matter Expertise for audits

Key Requirements

  • Bachelor's degree plus 10 years experience OR Master's plus 8 years OR PhD plus 6 years
  • Required: Medical writing or Pharmacovigilance (PV) experience
  • Working knowledge of drug development and post-marketing safety activities
  • Proven leadership skills to work in a matrix environment

Work Rights

Not specified

Tailored Resume

Cover Letter