Associate Director, Safety Data Sciences
Florham Park, NJ, United States
USD 126K-190K (estimate) Mid-level Full Time
Tasks
- Analyze safety data from literature
- Analyze safety data from safety databases
- Apply pharmacovigilance regulations and SOPs
- Author aggregate safety reports
- Communicate safety findings to product teams
- Conduct benefit risk impact assessment
- Evaluate safety signals
- Lead signal assessment material preparation
- Maintain safety sections of clinical documents
- Mentor and train safety scientists
- Perform safety signal detection
- Prepare safety summaries for safety meetings
- Prepare verbal safety updates
- Prepare written safety summaries
- Review safety data from clinical trials
- Support risk minimization activities
Perks/Benefits
Skills/Tech-stack
Aggregate Safety Reports | Benefit-risk assessment | Clinical study | Clinical study reports | Clinical trials | Database Review | Drug development | Epidemiology | Medical judgment | Microsoft Excel | Microsoft Word | Pharmacovigilance | Project Management | Regulatory Compliance | Risk Assessment | Risk Management | Risk Management Plan | Safety Database Review | Safety database | Safety reports | Signal Detection | Signal evaluation | Study Reports
Education
Bachelor of Science | Doctor of Pharmacy | Doctor of Philosophy | Master of Science | PhD
Regions
Countries
States
Cities
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