Head Of Pv & Drug Safety, West Coast Hub

Biogen

San Francisco, CA, United States
Base: $281,000.00-$387,000.00; bonus/equity: short...
Global safety surveillance expertise
Regulatory safety engagement
Pharmacovigilance strategy implementation
As the Head of Drug Safety & Pharmacovigilance for the West Coast Hub, you will ensure the safety and efficacy of therapies focused on immune-mediated diseases while leading global safety surveillance activities

Job Summary

  • As the Head of Drug Safety & Pharmacovigilance for the West Coast Hub, you will ensure the safety and efficacy of therapies focused on immune-mediated diseases while leading global safety surveillance activities.
  • The role offers a competitive base salary range of $281,000.00-$387,000.00 with eligibility for short and long-term incentives, comprehensive benefits, and a supportive work environment.
  • Biogen fosters a culture of inclusion, innovation, and collaboration, providing employees with opportunities for growth and the ability to make a significant impact in delivering life-changing medicines.

Matching Summary

As the Head of Drug Safety & Pharmacovigilance for the West Coast Hub, you will ensure the safety and efficacy of therapies focused on immune-mediated diseases while leading global safety surveillance activities.

Salary

Base: $281,000.00-$387,000.00; Bonus/Equity: Short and long-term incentives including cash bonus and equity opportunities; Benefits: Medical, dental, vision, life insurance, wellness programs, paid time off, 401(k) with match, stock purchase plan, tuition reimbursement

Skills & Requirements

Must-have

  • Global safety surveillance expertise
  • Regulatory safety engagement
  • Pharmacovigilance strategy implementation
  • Safety data evaluation and signal detection
  • Risk Management Plan development
  • Team leadership and mentoring
  • Safety databases and analytics proficiency

Nice-to-have

  • Strategic thinker
  • Cross-functional collaboration
  • Innovative safety surveillance
  • Executive communication skills
  • Culture of accountability and innovation
  • Experience with immune-mediated diseases
  • Fostering inclusion and belonging

Key Requirements

  • MD/PhD with post-graduate clinical training
  • 12+ years pharmacovigilance/drug safety experience
  • Expert knowledge of FDA/EMA regulations
  • Demonstrated global regulatory engagement success
  • Advanced pharmacoepidemiology or MPH preferred
  • Experience with immune-mediated or rare diseases
  • Domestic and international travel availability

Work Rights

Not specified

Tailored Resume

Cover Letter