SERM Medical Director - Immunology Safety

About the role

GSK is looking for a SERM Medical Director to provide medical and scientific leadership in the safety evaluation and risk management of its immunology assets in clinical development. The role interprets safety data, identifies and escalates safety signals and delivers evidence-based recommendations to support benefit-risk decisions, contributing to global governance and protecting patient safety. It is hybrid, based in the UK or Poland, with on-site presence for key meetings and governance activities.

Key responsibilities

• Lead pharmacovigilance and risk management for assigned immunology assets and clinical trials, defining strategy across the clinical development lifecycle
• Analyse and interpret clinical data and literature to identify and assess safety signals, and give expert medical input to global regulatory submissions
• Escalate safety concerns promptly in line with governance processes and represent Safety on cross-functional Clinical Matrix and project teams
• Lead cross-functional teams on urgent product safety issues and contribute to, or lead, Safety Review Teams
• Present safety issues and recommendations to senior governance committees and represent GSK with regulators, external experts and partners
• Help shape safety strategy for clinical programmes and SERM activities, and coach and mentor colleagues

Required profile

• Medical degree (or eligibility to practise in the UK) and relevant clinical experience, with formal postgraduate clinical training such as residency or specialty training
• Significant experience in pharmacovigilance, drug safety or medical affairs, with expertise in signal detection, evaluation and risk management
• Understanding of clinical development and post-marketing safety processes, and experience in matrixed, cross-functional environments
• Excellent written and verbal communication, including preparing medical and regulatory documents
• Preferred: postgraduate specialization, current GMC registration, immunology experience, regulatory submission and periodic safety report experience, knowledge of epidemiology, biostatistics or real-world evidence, and experience leading Safety Review Teams

What we offer

• Salary range of PLN 410,250 to PLN 683,750 for new hires in this position
• Possible annual bonus and eligibility for a share-based long-term incentive programme depending on role level
• Hybrid working model with remote work supported

To apply, submit a CV and a short note describing a safety assessment or risk management activity you led and its impact.