<span class="emphasis">Business Introduction</span><br />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.<br /><span class="emphasis">Find out more:</span><br /><a href="https://www.gsk.com/en-gb/innovation/" target="_blank">Our approach to R&D</a><br /><br /><span class="emphasis">Position Summary</span><div><div>Provides advanced scientific expertise in the safety evaluation and risk management of key GSK oncology assets in clinical development. Leads the identification, assessment, and communication of safety risks to ensure robust benefit-risk profiles and protection of patients globally.</div><div></div><div>This role plays a critical part in shaping the safety strategy of innovative oncology therapies, partnering cross-functionally to enable high-quality, timely decision-making and proactive risk mitigation across the portfolio.</div></div><br /><span class="emphasis">Key Responsibilities</span><div><h3><b>Scientific and Pharmacovigilance Leadership</b></h3>Lead pharmacovigilance activities and risk mitigation strategies for assigned oncology assets and clinical trialsDrive the evaluation and interpretation of safety data, including signal detection and assessmentDevelop strategic approaches for safety issue evaluation within clinical development programmesContribute to safety components of global regulatory submissions (e.g., INDs, DSURs, IBs)Perform literature review, clinical data synthesis, and integrated safety analyses to inform decision-makingEnsure high-quality, timely delivery while managing multiple priorities<h3><b>Cross-Functional Matrix Leadership</b></h3>Represent Safety Evaluation & Risk Management (SERM) on Clinical Matrix and Project TeamsLead cross-functional efforts to address urgent and complex product safety issuesPartner closely with Safety Physicians and stakeholders to prepare for and contribute to Safety Review Team (SRT) meetingsEscalate emerging safety issues to senior leadership and governance bodies as appropriateBuild strong working relationships and lead effectively within a global matrix organisationCoach and mentor colleagues as appropriate<h3><b>Communication, Influence and Strategy</b></h3>Present safety recommendations and emerging risks to senior governance committeesRepresent GSK in interactions with regulatory authorities, external experts, and partnersApply strategic thinking to evaluate internal and external factors influencing safety decisionsContribute to the development of long-term safety and clinical programme strategiesIdentify opportunities for continuous improvement and innovation in safety evaluation processesCommunicate complex scientific information clearly to a range of audiences</div><br /><span class="emphasis">Why You?</span><br /><br /><span class="emphasis">Basic Qualification</span><br />We are seeking professionals with the following required skills and qualifications to help us achieve our goals:<div>Degree in a health-related discipline (e.g., Life Sciences, Pharmacy, Medicine, Nursing), with significant relevant experienceSubstantial experience in pharmacovigilance, drug safety, or a related function within the pharmaceutical or biotechnology industryExperience supporting safety in oncology clinical development programmesStrong expertise in:Signal detection and risk assessmentClinical trial safety oversightRegulatory safety documentation and submissionsKnowledge of global pharmacovigilance regulations (e.g., ICH, GVP, CIOMS)Proven ability to work effectively in a complex, global matrix environmentStrong analytical, communication, and problem-solving skills</div><br /><span class="emphasis">Preferred Qualification</span><br />If you have the following characteristics, it would be a plus:<div>Advanced degree (e.g., PhD, PharmD, MD or equivalent)Experience interacting with global regulatory authoritiesExperience presenting to senior governance or safety review committeesDemonstrated leadership experience, including mentoring or team leadership in a matrix settingTrack record of influencing cross-functional teams and contributing to strategic decision-makingExperience supporting late-stage clinical development programmes</div><br /><span class="emphasis">Working arrangement</span><br />This is a hybrid role based in the United Kingdom with a mix of office and remote working. Some travel may be required for meetings and regulatory interactions.<br /><br /><span class="emphasis">What we value</span><br />We seek people who work with integrity, focus on patients and collaborate respectfully. We welcome different perspectives and promote inclusion in our teams. We support development and learning so you can grow while making a meaningful impact on patient safety.<br /><br /><span class="emphasis">Apply now</span><br />If you are ready to use your scientific expertise to protect patients and shape global safety strategy, we would like to hear from you. Please submit your CV and a short cover letter explaining what motivates you to take on this role.Belgium Salary Range / Fourchette salariale – Belgique: EUR 111,750 to EUR 186,250The 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.<b>Why GSK?</b><b>Uniting science, technology and talent to get ahead of disease together.</b> 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 <a target="_blank" href="mailto:UKRecruitment.Adjustments@gsk.com"><span style="color:#0000ff"><u>UKRecruitment.Adjustments@gsk.com</u></span></a> 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 <a target="_blank" href="https://www.gsk.com/en-gb/careers/how-we-hire/frequently-asked-questions/"><span style="color:#0000ff"><u>link</u></span></a> where you will find answers to multiple questions we receive <b>Important notice to Employment businesses/ Agencies</b>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. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at <a target="_blank" href="https://openpaymentsdata.cms.gov/"><span style="color:#0000ff"><u>https://openpaymentsdata.cms.gov/</u></span></a>
