Senior Pharmacovigilance Lead, West Coast Hub

Biogen

Remote, , US
Base: $198,000.00-$272,000.00; bonus/equity: cash ...
Pharmacovigilance vendor oversight
Global safety operations management
Adverse event assessment and reporting
As a Senior Pharmacovigilance Lead, you will oversee global safety operations and provide expert guidance across clinical development, regulatory filings, and post-marketing activities

Job Summary

  • As a Senior Pharmacovigilance Lead, you will oversee global safety operations and provide expert guidance across clinical development, regulatory filings, and post-marketing activities.
  • Biogen offers a competitive compensation package including base salary, short and long-term incentives, and a comprehensive benefits program supporting employees' physical, financial, emotional, and social well-being.
  • The company fosters a culture of inclusion and belonging, emphasizing diverse backgrounds and perspectives to strengthen innovation and teamwork.

Matching Summary

As a Senior Pharmacovigilance Lead, you will oversee global safety operations and provide expert guidance across clinical development, regulatory filings, and post-marketing activities.

Salary

Base: $198,000.00-$272,000.00; Bonus/Equity: Cash bonus and equity incentives available; Benefits: Medical, dental, vision, life insurance, paid vacation, parental leave, 401(k) match, tuition reimbursement

Skills & Requirements

Must-have

  • Pharmacovigilance vendor oversight
  • Global safety operations management
  • Adverse event assessment and reporting
  • Cross-functional safety governance
  • Safety data review and interpretation
  • Clinical development safety surveillance

Nice-to-have

  • Continuous improvement initiatives
  • Strategic benefit-risk assessments
  • Leadership in safety governance
  • Collaborative team environment
  • Scientific rigor and accountability
  • Strong communication and influence skills

Key Requirements

  • Bachelor's degree
  • 10+ years industry experience
  • 8+ years clinical/safety focus
  • Professional health background preferred
  • Knowledge of global safety regulations
  • Experience with MedDRA terminology
  • Experience authoring safety reports

Work Rights

Not specified

Tailored Resume

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