Serm Medical Director

GSK

United Kingdom
Hybrid
Safety evaluation and risk management
Pharmacovigilance
Clinical development and post-marketing
Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting

Job Summary

  • Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting.
  • Supports the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally.
  • You will expand your influence across global safety operations and develop skills in safety strategy, regulatory interactions and cross-functional leadership.

Matching Summary

Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting.

Skills & Requirements

Must-have

  • Safety Evaluation and Risk Management
  • Pharmacovigilance
  • Clinical development and post-marketing
  • Signal Detection and safety surveillance
  • International pharmacovigilance requirements

Nice-to-have

  • Cross-functional leadership
  • Agile working culture
  • Scientific rigour and collaboration
  • Mentoring scientific colleagues

Key Requirements

  • Medical degree
  • Formal postgraduate clinical training
  • Advanced experience in Pharmaceutical or Biotech industry
  • Significant pharmacovigilance experience
  • Experience with Signal Detection
  • Knowledge of international pharmacovigilance requirements
  • Experience working in large matrix organizations

Work Rights

Not specified

Tailored Resume

Cover Letter