Associate Director, Safety Analysis Scientist

Johnson & Johnson MedTech

Horsham, Pennsylvania, United States of America
Base: $137,000 to $235,750; bonus/equity: annual p...
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Safety evaluations and report writing
Medical writing and pharmacovigilance experience
Cross-functional collaboration in safety teams
** Johnson & Johnson MedTech is seeking an Associate Director, Safety Analysis Scientist, to lead safety assessments for various products in a hybrid role based in New Jersey or Pennsylvania. The ideal candidate will possess extensive experience in medical writing or pharmacovigilance, with a strong focus on oncology and related safety activities. **

Job Summary

  • The Associate Director Safety Analysis Scientist leads safety evaluations and collaborates with cross-functional teams to ensure regulatory compliance and product safety.
  • This role offers a hybrid work model requiring onsite presence three days a week across multiple US locations and includes competitive compensation with performance bonuses and comprehensive benefits.
  • Johnson & Johnson fosters an inclusive work environment valuing diversity and provides accommodations for applicants with disabilities.

Matching Summary

Match Score: 75

** Johnson & Johnson MedTech is seeking an Associate Director, Safety Analysis Scientist, to lead safety assessments for various products in a hybrid role based in New Jersey or Pennsylvania. The ideal candidate will possess extensive experience in medical writing or pharmacovigilance, with a strong focus on oncology and related safety activities. **

Salary

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

Skills & Requirements

Must-have

  • Safety evaluations and report writing
  • Medical writing and pharmacovigilance experience
  • Cross-functional collaboration in safety teams
  • Regulatory compliance and safety strategy
  • Data analysis and safety data review
  • Leadership in safety management teams
  • Proficiency in Microsoft Office applications

Nice-to-have

  • Clinical and oncology experience
  • Mentorship and training delivery
  • Innovative data presentation techniques
  • Experience with audits and inspections
  • Ability to influence and negotiate
  • Working in matrix environments

Key Requirements

  • Bachelor’s degree in healthcare or biomedical science
  • 11+ years industry experience or equivalent
  • Medical writing or pharmacovigilance experience required
  • Excellent English communication skills
  • Ability to analyze complex medical-scientific data
  • Leadership skills in matrix organizations
  • US work authorization required

Work Rights

US work authorization required

Tailored Resume

Cover Letter