SERM Medical Director

Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together.   Find out more: Our approach to R&D Position Summary  Provides medical and scientific leadership in the safety evaluation and risk management of GSK’s oncology assets in clinical development.  Responsible for the interpretation of safety data, identification and escalation of safety signals, and delivery of clear, evidence-based recommendations to support benefit–risk decisions. This role contributes to global governance and plays a critical part in protecting patient safety and shaping the safety profile of innovative oncology medicines.    Key Responsibilities  Scientific / Medical & Pharmacovigilance Expertise  Lead pharmacovigilance and risk management activities for assigned oncology assets and clinical trials  Define and drive strategy for the evaluation and management of safety issues across the clinical development lifecycle  Analyse and interpret clinical data, literature, and emerging evidence to identify and assess safety signals  Provide expert medical input into the safety components of global regulatory submissions  Apply sound clinical judgement to complex and sometimes conflicting data sets to inform benefit–risk decisions  Ensure timely escalation of safety concerns in line with governance processes    Matrix Leadership & Cross-functional Collaboration  Represent Safety on cross-functional Clinical Matrix and Project Teams  Lead cross-functional teams to address urgent and complex product safety issues  Actively contribute to and, where appropriate, lead Safety Review Teams (SRTs)  Build strong, collaborative relationships across functions and geographies  Coach and mentor colleagues, contributing to capability development within the organisation  Ensure effective communication and alignment with Safety Leads, senior SERM leadership, and key stakeholders    Communication, Influence & Governance  Lead presentations on safety issues and recommendations to senior governance committees  Influence decision-making through clear, credible, and evidence-based communication  Represent GSK in interactions with regulatory authorities, external experts, and partners  Contribute to the development of safety strategy for clinical programmes and broader SERM activities  Identify opportunities to improve processes, drive innovation, and enhance operational effectiveness  Operate with strong awareness of the internal and external regulatory and scientific environment    Why Join Us?  This is an opportunity to play a pivotal role in advancing GSK’s oncology pipeline, with direct impact on patient safety and global health outcomes.  You will:  Shape the safety strategy of innovative oncology medicines  Engage with senior governance and influence key development decisions  Work within a highly collaborative, global matrix environment  Contribute to scientific excellence and continuous improvement in safety science      Basic Qualifications  Medical degree with current GMC registration (or eligibility to practise in the UK) and relevant clinical experience  Completion of formal postgraduate clinical training (e.g., residency or specialty training)  Significant experience in pharmacovigilance, drug safety, or medical affairs  Demonstrated expertise in signal detection, evaluation, and risk management  Strong understanding of clinical development and post-marketing safety processes  Experience working effectively in matrixed, cross-functional environments  Excellent written and verbal communication skills, including preparation of medical and regulatory documents  Strong clinical judgement and the ability to deliver clear, evidence-based recommendations    Preferred Qualifications  Postgraduate specialisation in a clinical discipline or pharmaceutical medicine  Experience contributing to regulatory submissions and periodic safety reports  Knowledge of epidemiology, biostatistics, or real-world evidence relevant to safety assessment  Experience leading Safety Review Teams or acting as safety lead for major programmes  Prior engagement with regulatory authorities and external safety forums  Demonstrated ability to coach and develop colleagues in medical, scientific, or safety roles  Working Model This role is hybrid, based in the United Kingdom. You will be expected on site for key meetings, governance activities and team collaboration. Remote working is supported to balance focused work and stakeholder engagement. How to apply If this role speaks to you, please apply with your CV and a short note describing a safety assessment or risk management activity you led and its impact. If you need reasonable adjustments to apply or interview, tell us and we will support you. We welcome candidates from many backgrounds and encourage you to apply. Belgium Salary Range / Fourchette salariale – Belgique: EUR 119,250 to EUR 198,750The annual gross base salary range for new hires in this position is listed above for each applicable location. These ranges take into account a number of factors including the candidate’s skills, experience, education level and the market rate for the role. In addition, this position may offer an annual bonus and eligibility to participate in our share based long term incentive program which is dependent on the level of the role. More detailed information on the total benefits package will be supplied during the recruitment process. This role is available for applicants from multiple locations, and therefore salary ranges for certain locations are also shown. Salary ranges for other locations are shown because some markets have pay transparency laws that require salary information on job postings, and those locations are potential job sites for this role. If salary ranges are not displayed in the job posting for a specific location or country, the relevant compensation will be discussed during the recruitment process. Please note salaries vary by country based on the candidate’s skills, experience, education level and the market rate for the role. Offers are typically made within the advertised range based on the candidate’s skills, experience and qualifications, with the upper end generally reserved for highly experienced candidates or other exceptional circumstances aligned with these criteria. Why GSK? Uniting science, technology and talent to get ahead of disease together.   GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.   People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.   GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.   We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.   Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us at UKRecruitment.Adjustments@gsk.com where you can also request a call.   Please note should your enquiry not relate to adjustments, we will not be able to support you through these channels. However, we have created a  Recruitment FAQ guide. Click the link where you will find answers to multiple questions we receive   Important notice to Employment businesses/ Agencies GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. 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