Senior Medical Director, Oncology (Rock Island)

AbbVie in Rock Island, IL

  • Industry: Healthcare - Allied Health - Others
  • Type: Full Time
  • $122,260.00 - 195,330.00
position filled
  • Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance
  • Responsible for safety surveillance for pharmaceutical / biological / drug -device combined products
  • Contribute to the authorship of key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans
  • Apply current regulatory guidance as appropriate for safety surveillance and authorship of PV documents
  • Analyze and interpret aggregate safety data and communicate these analysis and interpretation to cross-functional teams
  • Effectively write, review and provide input on technical documents independently
  • Oversight and responsibility for leading the strategy for periodic reports (PSUR's, PADER's etc.)
  • Oversight of safety surveillance and pharmacovigilance activities for products in clinical trials and post marketing
  • Responsible for implementing risk management strategies for assigned products
  • Proactively engaging, inspiring, coaching and mentoring team and colleagues


  • MD / DO with 2+ years of residency with patient management experience
  • 5 - 8 years of Pharmacovigilance experience in the pharmaceutical industry
  • Ability to lead cross-functional team in a collaborative environment
  • Fluency, both written and oral, in English
  • Evaluate and make independent decisions
  • Work collaboratively and lead cross-functional teams
  • Write, review and provide input on technical documents
  • Effectively analyze and guide analysis of clinical data and epidemiological information
  • Effectively present recommendations / opinions in group environment both internally and externally
  • Master Public Health is preferred in addition to MD / DO, not required

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