Associate Director, Safety Analysis Scientist

J&J FAMILY OF COMPANIES

Horsham, Pennsylvania, United States of America
Base: $137,000 to $235,750; bonus/equity: annual p...
Hybrid (3 days onsite)
Safety evaluations and strategy discussions
Medical writing and pharmacovigilance experience
Cross-functional safety collaboration
Johnson & Johnson is seeking an Associate Director, Safety Analysis Scientist for a hybrid role located in New Jersey or Pennsylvania. The position entails leading safety assessments for drugs, collaborating with various stakeholders to ensure compliance and effective decision-making in safety management

Job Summary

  • The Associate Director Safety Analysis Scientist leads safety evaluations and collaborates with cross-functional teams to ensure high quality safety assessments for pharmaceutical products.
  • Johnson & Johnson provides an inclusive work environment respecting diversity and offers competitive compensation, benefits, and time off programs.
  • This hybrid role requires onsite presence three days a week at locations in Raritan, NJ; Titusville, NJ; or Horsham, PA, and supports global medical safety and regulatory interactions.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking an Associate Director, Safety Analysis Scientist for a hybrid role located in New Jersey or Pennsylvania. The position entails leading safety assessments for drugs, collaborating with various stakeholders to ensure compliance and effective decision-making in safety management.

Salary

Base: $137,000 to $235,750; Bonus/Equity: Annual performance bonus at company discretion; Benefits: Medical, dental, vision, life insurance, disability, retirement plans, and paid time off

Skills & Requirements

Must-have

  • Safety evaluations and strategy discussions
  • Medical writing and pharmacovigilance experience
  • Cross-functional safety collaboration
  • Safety data analysis and report writing
  • Regulatory compliance for safety
  • Leadership in safety management teams

Nice-to-have

  • Oncology experience
  • Clinical experience
  • Mentorship and training skills
  • Innovative data presentation
  • Matrix environment collaboration
  • Technical writing and communication

Key Requirements

  • Bachelor’s degree in healthcare or biomedical science
  • 11+ years industry experience or equivalent
  • Medical writing or pharmacovigilance experience
  • Excellent English communication skills
  • Ability to work in matrix environment
  • Proficiency in Microsoft Office applications

Work Rights

Not specified

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