Serm Medical Director

GSK

United Kingdom
Hybrid
Safety evaluation and risk management
Pharmacovigilance
Clinical development
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.
  • Leads Pharmacovigilance and Risk Management Planning and develops strategy for approach to evaluation of issues in the clinical matrix.
  • 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
  • Post-Marketing Activities
  • Signal Detection
  • Safety Surveillance

Nice-to-have

  • Cross-functional leadership
  • Agile working culture
  • Scientific rigor
  • Collaboration
  • Mentoring scientific colleagues

Key Requirements

  • Medical degree
  • Formal postgraduate clinical training
  • Advanced experience in Pharmaceutical/Biotech
  • Significant pharmacovigilance experience
  • Knowledge of international pharmacovigilance requirements
  • Experience in large matrix organizations

Work Rights

Not specified

Tailored Resume

Cover Letter