Senior Manager, Pharmacovigilance Agreements

Bilbao HR (Biogen?)

Research Triangle Park, NC, United States
Base: $134,000.00-$179,000.00; bonus/equity: short...
Safety data exchange agreements
Pharmacovigilance agreements
Global stakeholders collaboration
Collaborate with varied levels of cross-functional internal and external global stakeholders in all aspects of timely execution and maintenance of safety data exchange agreements (SDEAs) and pharmacovigilance agreements (PVAs) with Corporate Partners

Job Summary

  • Collaborate with varied levels of cross-functional internal and external global stakeholders in all aspects of timely execution and maintenance of safety data exchange agreements (SDEAs) and pharmacovigilance agreements (PVAs) with Corporate Partners.
  • This individual contributor role reports to the Head of PV Alliance Management (PVAM) and contributes directly to Biogen’s product pipeline and portfolio.
  • Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being.

Matching Summary

Collaborate with varied levels of cross-functional internal and external global stakeholders in all aspects of timely execution and maintenance of safety data exchange agreements (SDEAs) and pharmacovigilance agreements (PVAs) with Corporate Partners.

Salary

Base: $134,000.00-$179,000.00; Bonus/Equity: Short term and long-term incentives, cash bonus and equity incentive opportunities; Benefits: Medical, Dental, Vision, Life insurances, Fitness & Wellness programs, Disability insurance, Paid time off, Holidays, Paid Maternity and Parental Leave, 401(k) with match, ESPP, Tuition reimbursement

Skills & Requirements

Must-have

  • Safety data exchange agreements
  • Pharmacovigilance agreements
  • Global stakeholders collaboration
  • Audit and inspection readiness
  • GVP foundation

Nice-to-have

  • Emotionally intelligent contributor
  • Consensus building mindset
  • Continuous improvement mindset
  • Cross-functional relationships
  • Engaging others for optimal outcomes

Key Requirements

  • Bachelor’s degree in life sciences
  • 5 years of industry experience
  • Experience with safety agreements review
  • Excellent attention to detail
  • Strong oral and written communication
  • Familiar with drug development lifecycle

Work Rights

Not specified

Tailored Resume

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