Serm Associate Scientific Director

GSK

Competitive salary; annual bonus based on compyny ...
Hybrid
Health sciences or health care professional degree
Substantial pharmacovigilance experience
Safety evaluation and risk management expertise
GSK is seeking a Serm Associate Scientific Director to provide medical and scientific expertise in safety evaluation and risk management for clinical development and post-marketing assets. The role requires substantial experience in pharmacovigilance, with a focus on signal detection, regulatory reporting, and cross-functional collaboration. The position offers a hybrid work model and competitive benefits, emphasizing a culture that supports professional growth and inclusivity

Job Summary

  • The role provides medical and scientific expertise in the safety evaluation and risk management of key GSK assets in both clinical development and post-marketing settings.
  • Candidates will drive the production of regulatory periodic reports, Risk Management Plans (RMPs), and author SERM safety contributions to global regulatory submissions.
  • GSK offers a competitive salary, annual bonus based on company performance, healthcare programs, pension plan membership, and a hybrid working model through the Performance with Choice programme.

Matching Summary

Match Score: 85

GSK is seeking a Serm Associate Scientific Director to provide medical and scientific expertise in safety evaluation and risk management for clinical development and post-marketing assets. The role requires substantial experience in pharmacovigilance, with a focus on signal detection, regulatory reporting, and cross-functional collaboration. The position offers a hybrid work model and competitive benefits, emphasizing a culture that supports professional growth and inclusivity.

Salary

Competitive salary; Annual bonus based on company performance; Healthcare, wellbeing programmes, pension, shares and savings

Skills & Requirements

Must-have

  • Health Sciences or Health Care Professional degree
  • Substantial pharmacovigilance experience
  • Safety evaluation and risk management expertise
  • Knowledge of ICH GVP modules and CIOMS initiatives
  • Experience with international drug development processes

Nice-to-have

  • Advanced degree preferred
  • Matrix organization experience
  • Cross-functional leadership skills
  • Process improvement initiative participation

Key Requirements

  • BSc, MS, PhD, RN/BSN/MSN, NP, RPh/B Pharm/Pharm D required
  • Substantial experience in pharmacovigilance or drug development
  • Experience with international pharmacovigilance requirements (ICH, GVP)

Work Rights

Not specified

Tailored Resume

Cover Letter