Serm Associate Scientific Director

GlaxoSmithKline

Competitive salary; annual bonus based on compyny ...
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Health sciences or health care professional degree required
Substantial experience in pharmacovigilance
Experience with safety evaluation and risk management
** GlaxoSmithKline is seeking a Serm Associate Scientific Director to provide medical and scientific expertise in safety evaluation and risk management for their clinical development assets. The role emphasizes collaboration, data analysis, and regulatory compliance, all while supporting the company's mission to enhance patient safety globally. **

Job Summary

  • This role provides medical and scientific expertise in the safety evaluation and risk management of key GSK assets in clinical development and post-marketing settings.
  • The position involves driving the production of regulatory periodic reports, Risk Management Plans (RMPs), and authoring SERM safety contributions to global regulatory submissions.
  • GSK offers a competitive salary, annual bonus, healthcare programs, pension plan membership, shares and savings program, and a hybrid working model.

Matching Summary

Match Score: 75

** GlaxoSmithKline is seeking a Serm Associate Scientific Director to provide medical and scientific expertise in safety evaluation and risk management for their clinical development assets. The role emphasizes collaboration, data analysis, and regulatory compliance, all while supporting the company's mission to enhance patient safety globally. **

Salary

Competitive salary; Annual bonus based on company performance; Benefits include healthcare, pension, and shares

Skills & Requirements

Must-have

  • Health Sciences or Health Care Professional degree required
  • Substantial experience in pharmacovigilance
  • Experience with Safety Evaluation and Risk Management
  • Knowledge of international pharmacovigilance requirements
  • Experience with ICH, GVP modules, and CIOMS initiatives

Nice-to-have

  • Advanced degree preferred
  • Matrix leadership experience
  • Process improvement initiative participation
  • Strong communication and influencing skills

Key Requirements

  • BSc, MS, PhD, RN/BSN/MSN, NP, RPh/B Pharm/Pharm D degree
  • Substantial pharmacovigilance experience
  • International pharmacovigilance knowledge (ICH, GVP, CIOMS)

Work Rights

Not specified

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