Scientific Director, Oncology - Global Patient Safety

Added
19 days ago
Type
Full time
Salary
Upgrade to Premium to se...

Related skills

cross-functional collaboration regulatory affairs clinical trials pharmacovigilance oncology

πŸ“‹ Description

  • Support the planning and execution of the safety strategy for Oncology assets during the entire
  • Supports the Safety Leads and Product Safety Teams (PSTs) to translate nonclinical and clinical
  • May lead development and implementation of an asset safety strategy with support of PST-L or
  • Leads the review and synthesis of scientific safety data for critical regulatory and clinical
  • Facilitate scientific connections and interactions, info exchange across assets within the safety
  • Prepare material on competitive intelligence, current disease state and standard of care for key

🎯 Requirements

  • Scientific or clinical degree (e.g. NP/PA, PharmD, MS, PhD, MPH, including combinations)
  • 5+ years of experience in Pharmacovigilance / Clinical Development / Development biological
  • Proven ability to critically evaluate and interpret complex safety data from oncology clinical
  • Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical
  • Ability to exercise judgment and address complex problems and create solutions across multiple
  • Must be able to lead and manage through influence.

🎁 Benefits

  • Paid time off (vacation, holidays, sick)
  • Medical/dental/vision insurance
  • 401(k) plan
  • Long-term incentive programs
Share job

Meet JobCopilot: Your Personal AI Job Hunter

Automatically Apply to Engineering Jobs. Just set your preferences and Job Copilot will do the rest β€” finding, filtering, and applying while you focus on what matters.

Related Engineering Jobs

See more Engineering jobs β†’