Associate Director, Safety Scientist

BeiGene

Base: $154,300.00 - $204,300.00 annually; bonus/eq...
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Pharmd or phd in medical field
4+ years pharmacovigilance experience
Signal detection and assessment
** BeiGene is seeking an Associate Director, Safety Scientist, to lead safety science activities focused on early and late-stage clinical development. The ideal candidate will have a strong background in pharmacovigilance, safety data analysis, and communication, contributing to the company's mission of advancing cancer therapeutics. **

Job Summary

  • This role focuses on early development (phase I) and late stage (phase II-III) safety science activities for a global biotechnology company fighting cancer.
  • The position requires leading signal evaluation, safety monitoring, and the preparation of critical regulatory documents like Investigator Brochures and Package Inserts.
  • BeOne offers a comprehensive benefits package including medical, dental, vision, 401(k), and discretionary equity awards to all employees.

Matching Summary

Match Score: 75

** BeiGene is seeking an Associate Director, Safety Scientist, to lead safety science activities focused on early and late-stage clinical development. The ideal candidate will have a strong background in pharmacovigilance, safety data analysis, and communication, contributing to the company's mission of advancing cancer therapeutics. **

Salary

Base: $154,300.00 - $204,300.00 annually; Bonus/Equity: Eligible for annual bonus plan and discretionary equity awards; Benefits: Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, PTO, Wellness

Skills & Requirements

Must-have

  • PharmD or PhD in medical field
  • 4+ years pharmacovigilance experience
  • Signal detection and assessment
  • MedDRA knowledge
  • Safety database retrieval skills

Nice-to-have

  • Collaborative team spirit
  • Bold ingenuity mindset
  • Patient-first approach
  • Cross-functional collaboration
  • Data mining tools familiarity

Key Requirements

  • PharmD, PhD, RN, or MD degree required
  • 4+ years analytical pharmacovigilance experience
  • 2+ years pharmaceutical industry experience preferred
  • Board eligibility or certification for US physicians
  • Advanced MS Office and MedDRA proficiency

Work Rights

Not specified

Tailored Resume

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