Medical Director- Early Development Oncology

Added
15 days ago
Type
Full time
Salary
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Related skills

risk management technical writing regulatory affairs epidemiology clinical data analysis
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📋 Description

  • Responsible for supporting the Product Safety Lead (PST) in ensuring safety in one or more products
  • Interpreting regulations related to pharmacovigilance supporting all patient safety activities.
  • Understanding and application of the pharmacology, chemistry and non-clinical toxicology to
  • Safety surveillance for pharmaceutical / biological / drug –device combined products.
  • Contribute to the authorship of key pharmacovigilance documents, including but not limited to
  • Apply current regulatory guidance as appropriate for safety surveillance and authorship of PV

🎯 Requirements

  • MD / DO with 2+ years of residency with patient management experience required
  • Master Public Health is preferred in addition to MD / DO
  • Effectively analyze clinical data and epidemiological information required
  • Effectively write technical documents with direction
  • Work collaboratively in a team environment and be self-starting and able to work independently
  • Ability to effectively present recommendation / opinions in group environment

🎁 Benefits

  • Paid time off (vacation, holidays, sick)
  • Medical/dental/vision insurance
  • 401(k)
  • Eligible to participate in long-term incentive programs
  • Comprehensive benefits package
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