IrvineFull TimeOther
Remotely
pharmacovigilancerisk managementdataregulatorypsursignal detectionsafety dataclinical summary of safetysafety data sciences
Job Description
📋 Description
- Lead surveillance for a product’s lifecycle across assigned compounds
- Partner with safety and clinical teams for signal assessments
- Prepare materials for regulatory safety requests
- Assess safety issues and impact on benefit-risk
- Communicate findings to inform risk minimization strategies
- Authors safety sections in CSRs, PSURs, and risk documents
🎯 Requirements
- Health sciences degree (PharmD/PhD/MPH) or Bachelor + 4 yrs safety experience
- Knowledge of drug development and regulatory submission processes
- Experience with safety evaluation tools and cross-functional collaboration
- Strong oral/written communication and multitasking ability
- Proficiency in MS Word/Excel and basic project mgmt
- Ability to work independently in a matrix team
🎁 Benefits
- Competitive compensation and comprehensive benefits
- Long-term incentive programs eligibility
- Paid time off and medical/dental/vision insurance
- 401(k) plan with company match
- AbbVie Equal Opportunity Employer
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