IrvineFull TimeHealthcare
Remotely
pharmacovigilanceregulatory submissionsndapsurdsurpadersnda
Job Description
📋 Description
- Lead safety strategy for late-stage oncology products within the Product Safety Team (PST).
- Ensure safety across the product lifecycle: surveillance, signal detection, risk management, and
- Collaborate with PK, toxicology, regulatory, clinical development, and medical affairs to guide
- Interpret regulations related to pharmacovigilance and author PV documents; lead periodic reporting
- Mentor and coach team members; contribute to publications and safety leadership initiatives.
- Engage cross-functionally in a fast-paced environment with strong teamwork and communication.
🎯 Requirements
- MD/DO with 2+ years of internal medicine/patient management; PhD or Clinical Pharmacology
- 2-5 years of Pharmacovigilance/Clinical Development in pharma; experience supporting regulatory
- Oncology patient safety experience required; ability to lead cross-functional teams and present
- Strong analytical and writing skills for technical documents; regulatory knowledge in PV is
🎁 Benefits
- AbbVie offers a comprehensive package including paid time off, medical/dental/vision insurance, and
- Eligible to participate in long-term incentive programs.
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