4 часа назад
Associate Director, Safety Analysis Scientist (MedTech)
137 000 - 235 750$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
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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