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4 часа назад

Associate Director, Safety Analysis Scientist (MedTech)

137 000 - 235 750$
Формат работы
hybrid
Тип работы
fulltime
Грейд
director
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Associate Director, Safety Analysis Scientist (MedTech): Leading scientific safety assessments, analyses, reports, and risk-management activities for marketed and developing products with an accent on pharmacovigilance, regulatory compliance, and cross-functional safety strategy. Focus on interpreting complex medical-scientific data, leading proactive safety reviews, supporting health-authority interactions, and influencing product safety decisions.

Location: Hybrid role based in Horsham, Pennsylvania, Raritan, New Jersey, or Titusville, New Jersey, United States

Base pay: $137,000–$235,750 per year

Company

Johnson & Johnson MedTech develops healthcare and medical solutions, while the broader organization advances medicines and technologies for complex diseases.

What you will do

  • Lead scientific safety evaluations, including strategy discussions, data retrieval and analysis, report writing, and revisions.
  • Support Product Safety Management Teams by preparing and presenting data, maintaining signal tracking, and compiling meeting materials.
  • Lead proactive safety data reviews and develop safety positions for use in aggregate safety reports.
  • Provide written and verbal support for Health Authority interactions involving safety and risk management.
  • Review regulatory and clinical documents, oversee complex deliverables, and provide product or process subject-matter expertise for audits and inspections.
  • Lead cross-functional training and initiatives, improve data presentation and reporting efficiency, and act as a backup to the Therapeutic Area Lead when needed.

Requirements

  • Bachelor’s degree in healthcare-related or biomedical science with 11+ years of industry experience, or an advanced degree with 8+ years of experience.
  • Required experience in medical writing or pharmacovigilance; clinical experience is preferred.
  • Working knowledge of medical concepts, safety activities in drug development and post-marketing, and global health-authority requirements.
  • Ability to analyze complex medical-scientific data and interpret benefit-risk impact.
  • Excellent English verbal and written communication skills.
  • Leadership, stakeholder-management, planning, prioritization, negotiation, and Microsoft Office proficiency.

Culture & Benefits

  • Inclusive work environment guided by the company’s Credo and equal-opportunity principles.
  • Eligibility for pension and 401(k) savings plans.
  • Eligibility for the long-term incentive program.
  • Vacation, sick time, holidays, personal and family time, parental leave, caregiver leave, bereavement leave, volunteer leave, and military spouse time-off benefits.
  • Inclusive interview accommodations are available for applicants with disabilities.

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