Associate Director, Safety Analysis Scientist

Job Title Associate Director, Safety Analysis Scientist (Hybrid) Location Raritan, NJ; Titusville, NJ; Horsham, PA Purpose The Associate Director Safety Analysis Scientist (AD SAS) provides scientific expertise and leads safety assessments of assigned products. The AD SAS works with the Medical Safety Officer (MSO) and Safety Management Teams (SMTs) to prepare scientific safety analysis and evaluations for regulatory compliance and safety‑related decisions. Responsibilities Lead safety evaluations, including strategy discussions, data retrieval, analysis, report writing, and revisions. Ensure high‑quality safety evaluations and reports with minimal stakeholder comments. Provide input and review of key regulatory or clinical documents. Support SMT activities: data preparation, presenting data, meeting minutes, signal‑tracking updates. Lead proactive safety data reviews and develop safety positions for Global Medical Safety (GMS). Support Health Authority interactions, both written and verbal. Own novel projects, innovate processes, and optimize reporting efficiency. Train and oversee cross‑functional stakeholders and other team members on safety deliverables. Act as Subject Matter Expert for audits and inspections. Participate in department and cross‑functional initiatives. Assist Directors with controlled document creation, review, and implementation. Manage unscheduled reports within the Aggregate Report Calendar. Line‑manage contractor positions, as applicable. Act as backup to the Therapeutic Area Lead when needed. Qualifications Education: Bachelor’s degree in Healthcare‑related or Biomedical Science (minimum 11 years industry experience) or Advanced degree with 8 years experience. Experience: Medical writing or Pharmacovigilance (PV) with working knowledge of safety activities in drug development, post‑marketing, and global Health Authority requirements. Skills: Analyze complex medical‑scientific data; present benefit‑risk impact; excellent English communication; stakeholder interaction; matrix environment leadership; project planning; Microsoft Office proficiency. Preferred: Clinical experience; Oncology experience. Compensation and Benefits The anticipated base pay range in the United States is $137,000 to $235,750. Additional benefits include medical, dental, vision, life insurance, disability coverage, retirement plans (401(k)), and paid time off. The position is eligible for an annual performance bonus. EEO Statement Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities. Application Deadline March 12th, 2026. #J-18808-Ljbffr