Senior Medical Director, Safety and Regulatory Affairs

6 days ago


Irvine, California, United States AbbVie Full time
Job Summary

The Medical Director, Device Safety and Surveillance will play a critical role in ensuring the safety of our medical devices and products. This individual will be responsible for supporting the Product Safety Leads and potentially leading the safety surveillance efforts for one or more products.

Key Responsibilities
  • Surveillance and Signal Detection: The Medical Director will be responsible for conducting safety surveillance and detecting potential signals related to our medical devices and products.
  • Regulatory Compliance: This individual will ensure that all safety-related activities are in compliance with relevant regulations and guidelines.
  • Document Authorship: The Medical Director will contribute to the authorship of key pharmacovigilance documents, including medical safety assessments, regulatory responses, and risk management plans.
  • Team Leadership: This individual will lead cross-functional teams and provide guidance on safety-related matters.
  • Qualifications: The ideal candidate will have a medical degree (MD or DO) with 2+ years of residency experience and a Master's degree in Public Health (MPH) or a related field. Additionally, 2-4 years of experience in pharmacovigilance in the pharmaceutical industry is required.
What We Offer
  • Competitive Compensation: AbbVie offers a comprehensive compensation package, including a competitive salary and benefits.
  • Opportunities for Growth: As a Medical Director at AbbVie, you will have opportunities to grow and develop your career in a dynamic and supportive environment.
  • Diversity and Inclusion: AbbVie is committed to diversity and inclusion and welcomes applications from qualified individuals from diverse backgrounds.


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