Senior Safety Data Scientist
Florham Park, NJ, United States
USD 127K-230K (estimate) Senior-level Full Time
Tasks
- Analyze data from multiple sources
- Assess benefit risk impact using medical judgment
- Author and review aggregate safety reports
- Communicate surveillance findings to product teams
- Conduct safety signal detection
- Contribute to Clinical Summary of Safety
- Contribute to Company Core Data Sheets
- Contribute to clinical study reports
- Contribute to risk management plan
- Develop global aggregate safety reports
- Develop signal assessment strategies
- Evaluate safety signals
- Perform standard safety surveillance
- Prepare summaries of key safety data for safety meetings
- Prepare verbal safety summaries
- Prepare written safety summaries
- Review safety data from clinical trials
- Review safety data from literature
- Review safety data from safety databases
- Support ad hoc regulatory safety requests
Perks/Benefits
Skills/Tech-stack
Basic project management | Benefit-risk assessment | Clinical trials | Development Process | Drug Safety | Drug Safety Surveillance | Drug development | Drug development process | Management planning | Medical judgment | Microsoft Excel | Microsoft Word | Pharmacovigilance | Project Management | Regulatory Submissions | Risk Assessment | Risk Management | Risk management planning | Safety Surveillance | Signal Detection | Signal evaluation
Education
Bachelor of Engineering | Bachelor of Science | Master of Science | PhD
Regions
Countries
States
Cities
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