Senior Safety Evaluation Scientist -iii Literature

gssi.world

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Pharmacovigilance
Drug safety
Literature screening
** GSK is seeking a Senior Safety Evaluation Scientist to perform safety literature assessments and contribute to pharmacovigilance activities in alignment with regulatory requirements. The ideal candidate will have a life sciences background, extensive experience in pharmacovigilance, and strong communication skills. **

Job Summary

  • Perform Safety literature assessment activities for signal detection and aggregate reports purposes in accordance with their procedures and regulatory requirements.
  • The position holder is responsible for the above elements in alignment with GSK standards and regulatory timelines whilst driving the implementation of robust processes for successful PV operations activities, including vendor oversight.
  • We welcome different perspectives and create an environment of inclusion where everyone can bring their best.

Matching Summary

Match Score: 75

** GSK is seeking a Senior Safety Evaluation Scientist to perform safety literature assessments and contribute to pharmacovigilance activities in alignment with regulatory requirements. The ideal candidate will have a life sciences background, extensive experience in pharmacovigilance, and strong communication skills. **

Skills & Requirements

Must-have

  • pharmacovigilance
  • drug safety
  • literature screening
  • signal detection
  • regulatory requirements
  • process improvement

Nice-to-have

  • ambitious for patients
  • accountable for impact
  • doing the right thing
  • inclusive environment
  • patient safety first

Key Requirements

  • Bachelor’s degree in life sciences
  • Minimum 7 years’ experience
  • Pharmaceutical industry experience
  • Basic knowledge of post-marketing regulations
  • Knowledge of causality assessment principles
  • Working knowledge of pharmacovigilance regulations

Work Rights

Not specified

Tailored Resume

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