Associate Director, Structured Benefit-risk Assessment Lead

Bristol Myers Squibb

Not specified; not specified; competitive benefits...
Hybrid (50% onsite)
Structured benefit-risk assessment frameworks
Global pharmacovigilance expertise
Cross-functional team leadership
Bristol Myers Squibb is seeking an Associate Director for Structured Benefit-Risk Assessment Lead to oversee benefit-risk assessments across their portfolio. The role involves leading cross-functional teams and requires extensive experience in pharmacovigilance and safety risk management

Job Summary

  • This role serves as the go-to expert for benefit-risk methodology, leading cross-functional teams to shape company-wide positions on medicine profiles.
  • The position requires guiding end-to-end benefit-risk assessments from early clinical development through post-marketing stages while championing the patient voice.
  • Bristol Myers Squibb offers a wide variety of competitive benefits and programs designed to support employees in pursuing their goals both at work and in personal lives.

Matching Summary

Match Score: 85

Bristol Myers Squibb is seeking an Associate Director for Structured Benefit-Risk Assessment Lead to oversee benefit-risk assessments across their portfolio. The role involves leading cross-functional teams and requires extensive experience in pharmacovigilance and safety risk management.

Salary

Not specified; Not specified; Competitive benefits and programs offered

Skills & Requirements

Must-have

  • Structured benefit-risk assessment frameworks
  • Global pharmacovigilance expertise
  • Cross-functional team leadership
  • Regulatory compliance knowledge
  • Patient preference study integration

Nice-to-have

  • Creative problem-solving abilities
  • Stakeholder management skills
  • Publication authoring experience
  • Conflict resolution capabilities
  • Strategic vision development

Key Requirements

  • BS/BA required with advanced degree preferred
  • 10+ years pharmaceutical or healthcare industry experience
  • Significant expertise in global pharmacovigilance
  • Strong knowledge of global regulatory frameworks

Work Rights

Not specified

Tailored Resume

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