Director Of Drug Safety(physician)

Systimmune Inc

Princeton, NJ, United States
Base: $200,000 - $300,000 annually; bonus/equity: ...
On-site
Medical assessment of safety data
Cross-functional team collaboration
Drug safety regulations knowledge
Systimmune Inc is seeking a Director of Drug Safety with a medical background to oversee safety data assessment in clinical trials, focusing on oncology and hematology. The role requires extensive experience in drug safety and pharmacovigilance, along with a strong understanding of US and EU regulations

Job Summary

  • This individual is to lead medical assessment and interpretation of safety data from multiple sources, including clinical trials, and literature reports.
  • The individual will be closely collaborating with cross functional teams in supporting all clinical development programs, regulatory filling, and global safety related activities.
  • SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.

Matching Summary

Match Score: 85

Systimmune Inc is seeking a Director of Drug Safety with a medical background to oversee safety data assessment in clinical trials, focusing on oncology and hematology. The role requires extensive experience in drug safety and pharmacovigilance, along with a strong understanding of US and EU regulations.

Salary

Base: $200,000 - $300,000 annually; Bonus/Equity: Not specified; Benefits: 100% paid employee premiums for medical/dental/vision, STD, LTD, 401(k) with 50% company match up to 3%, 15 PTO days, sick leave, 11 paid holidays

Skills & Requirements

Must-have

  • medical assessment of safety data
  • cross-functional team collaboration
  • drug safety regulations knowledge
  • pharmacovigilance practices
  • safety surveillance and risk management

Nice-to-have

  • learning and growth opportunities
  • cutting-edge biologics development
  • contribute to company success

Key Requirements

  • 5+ years' experience in Drug Safety/Pharmacovigilance
  • Medical Degree (MD)
  • Oncology / Hematology experience preferred
  • Strong working knowledge of US and EU drug safety regulations
  • Proficiency with medical review of ICSRs

Work Rights

Not specified

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