Hybrid Senior Scientific Director

Posted 19 hours ago

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About the role

  • Leading Safety and Pharmacovigilance initiatives within GSK. Overseeing clinical safety evaluation and driving risk management strategies globally.

Responsibilities

  • Lead medical and scientific staff within the SERM.
  • Implement policy, processes and support operational and strategic plans.
  • Ensure scientifically sound review and interpretation of data.
  • Coaches and mentors SERM colleagues in signal evaluation methodology and risk management.
  • Champions/sponsors safety governance by developing safety strategy for products.

Requirements

  • Expert in clinical safety and pharmacovigilance activities.
  • Demonstrated record of sound judgement and decision making in safety evidence generation, benefit-risk assessment, causality assessment, evaluation of safety signals.
  • Excellent medical/scientific judgment, strong analytical skills.
  • Champions/sponsors safety governance by development of safety strategy.
  • Proven ability to affect department, or product strategies with a strong understanding of global considerations.

Benefits

  • Health Sciences/Health Care Professional degree required (e.g., BSc, MS, PhD, RN/BSN/MSN, NP, RPh/B Pharm/Pharm D)
  • Relevant pharmacovigilance, drug safety or safety evaluation experience in industry.
  • Experience covering both clinical development and post-marketing safety activities, including signal detection and risk management.
  • Demonstrated familiarity with global pharmacovigilance regulations and guidance (for example, EU GVP and international standards).
  • Proven experience working and influencing effectively in a matrix organisation.
  • Strong scientific writing, presentation and interpersonal communication skills.

Job title

Senior Scientific Director

Job type

Experience level

Senior

Salary

Not specified

Degree requirement

Postgraduate Degree

Location requirements

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