Serm Senior Scientific Director

GSK

United Kingdom
Hybrid
Clinical safety and pharmacovigilance
Benefit-risk assessment
Safety signal evaluation
Responsible to lead medical and scientific staff within the SERM (Safety Evaluation & Risk Management) and defining and driving the strategy and vision of clinical safety and pharmacovigilance activities in alignment with Global Safety business strategies

Job Summary

  • Responsible to lead medical and scientific staff within the SERM (Safety Evaluation & Risk Management) and defining and driving the strategy and vision of clinical safety and pharmacovigilance activities in alignment with Global Safety business strategies.
  • Focus on efficiency and effectiveness to meet the needs of our Patients and HCPs, supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally.
  • You will have opportunities to develop your leadership, broaden your scientific impact, and contribute to change that benefits patients worldwide.

Matching Summary

Responsible to lead medical and scientific staff within the SERM (Safety Evaluation & Risk Management) and defining and driving the strategy and vision of clinical safety and pharmacovigilance activities in alignment with Global Safety business strategies.

Skills & Requirements

Must-have

  • clinical safety and pharmacovigilance
  • benefit-risk assessment
  • safety signal evaluation
  • risk management strategies
  • global pharmacovigilance regulations

Nice-to-have

  • ambitious for patients
  • accountable for impact
  • collaborative working
  • agile working culture

Key Requirements

  • Health Sciences/Health Care Professional degree
  • Relevant pharmacovigilance experience
  • Experience in clinical development and post-marketing
  • Familiarity with global PV regulations
  • Experience influencing in a matrix organisation

Work Rights

Not specified

Tailored Resume

Cover Letter