The Urology Account Manager is accountable for appropriate product adoption across targeted Urology accounts to drive sales.
\nKey Responsibilities:
\nBasic Qualifications:
\nPreferred Qualifications:
\nWe are seeking a Cancer Vaccine Asset Lead to collaborate with stakeholders to create strategies that support the organisational vision and ensure quality and compliance oversight for the cancer vaccine program.
\nThe successful candidate will serve as the asset's single point of contact and spokesperson to senior management and senior boards, and increase visibility among external communities to bring cancer vaccine solutions to patients with unmet medical needs.
\nKey responsibilities include:
\nThe ideal candidate will have:
\nPreferred qualifications include:
\nIn terms of compensation, the annual base salary for new hires in this position ranges from $340,500 to $567,500, depending on location and experience. The company also offers an annual bonus and eligibility to participate in a share-based long-term incentive program, as well as comprehensive benefits, including healthcare and insurance benefits, retirement benefits, paid holidays, and paid caregiver/parental and medical leave.
","enriched_at":1792942395363},{"id":"job_2ee6c90b-0e2","title":"Senior Principle Owner – Observability","source_url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/Bengaluru-Luxor-North-Tower/Cloud---Hosting---Senior-Product-Owner---Observability_449216","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"Engineering","description":"The Senior Principle Owner – Observability owns GSK's enterprise observability platform as a product. This is a techno-functional role that sets the product vision, owns and orders the backlog, and is hands-on enough to configure BindPlane and OpenTelemetry pipelines, write parsing rules, script ingestion utilities, build Grafana dashboards, and debug issues.
\nThe role leads the platform's back-end migration from self-managed Prometheus/Mimir and Elastic SaaS to Google Cloud Observability. The goal is to deliver a platform that teams adopt by choice, with features such as onboarding through golden templates, SLOs that reflect business needs, and alerting that cuts noise.
\nKey responsibilities:
\nRequirements:
\nNice to have:
\nJoin GSK as an Associate Director, Global Epidemiology and Real-World Evidence, and lead epidemiology efforts that shape evidence across development and lifecycle activities.
\nYou will work with clinical development, safety, regulatory, outcomes, and commercial partners to design and deliver epidemiologic studies using real-world data, registries, and other sources.
\nThis role offers growth, visible impact on decisions that matter for patients, and a chance to help unite science, technology, and talent to get ahead of disease together.
\nResponsibilities:
\nBasic Qualifications & Skills:
\nPreferred Qualifications & Skills:
\nBenefits:
\nThe Senior Manager, Product Management – Field Intelligence is responsible for the technology strategy, roadmap, architecture, delivery, lifecycle management, and operational excellence of GSK's unified Field Intelligence platform supporting the US Commercial organization.
\nThis role serves as the Technology Product Manager for the end-to-end Field Intelligence ecosystem, transforming trusted commercial data into actionable insights, recommendations, and AI-powered experiences that improve field effectiveness and decision-making.
\nThe Senior Manager is accountable for the technology product across the full data-to-experience stack, partnering with Data Engineering, Data Architecture, Enterprise Architecture, AI Engineering, Analytics, Cloud and Platform Engineering, CRM Engineering, Commercial stakeholders, and external technology partners.
\nResponsibilities
\nBasic Qualification
\nWe are seeking a Senior Manager, Product Management – Core CRM to lead the technology strategy, roadmap, architecture, lifecycle management, and operational excellence of GSK’s US Vault CRM platform and Core CRM product ecosystem.
\nThe Senior Manager will be responsible for:
\nThe ideal candidate will have:
\nWe offer a comprehensive benefits program, including:
\n#GSK-LI #AGTech
","enriched_at":1792942070959},{"id":"job_d4a78150-4ac","title":"Senior Major Incident Manager","source_url":"https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/Durham-Blackwell-Street/RE---Operations---Lead-Major-Incident-Mngr-_449002","location":null,"job_type":"full-time","experience_level":"senior","work_arrangement":null,"category":"IT","description":"The Digital & Tech Command Centre operates 24x7x365 to protect GSK's critical sites, applications, and services. The Senior Major Incident Manager role owns and leads the end-to-end response to Major Incidents (P1) and managed high-priority (P2) incidents.
\nKey Responsibilities
\nRequirements
\nNice to Have
\nMake a difference in oncology care,where science meets patient impact
\nAt GSK, we are united by a shared ambition: to get ahead of disease together. We are seeking an experienced and strategic Medical Affairs Lead (Oncology) to lead our oncology medical strategy in Malaysia across solid tumours and haematology.
\nThis is a high-impact leadership role responsible for shaping scientific strategy, driving launch readiness, and strengthening external partnerships to improve patient outcomes.
\nYour Impact
\nAs Medical Affairs Lead, you will:
\nWhy this role matters
\nYou will play a pivotal role in bringing innovative oncology therapies to patients in Malaysia, strengthening access, improving diagnostic pathways, and ensuring evidence-based decision-making across the healthcare ecosystem.
\nAbout You
\nWe are looking for a leader who combines strong scientific expertise with strategic thinking:
\nBenefits
\nAs a GSK Medical Science Liaison (MSL), you will function as a key scientific resource for Canadian hepatology and GI specialists.
\nYour three core responsibilities are: 1) Responding to requests for in-depth scientific information in the field of hepatology; 2) Discussing and contextualizing new data from scientific conferences, publications, and GSK's pipeline to ensure a strong external understanding of how the science fits into clinical practice; 3) Driving the capture of important scientific insights from the external environment to support GSK's research efforts and inform overall medical strategy.
\nResponsibilities This role will provide you with the opportunity to lead key activities to progress your career. These responsibilities include:
\nRequirements
\nPreferred Qualifications
\nThe Attach and Train Programme (AnT) is a 15-month structured on-the-job training programme designed to build a pipeline of skilled professionals for Singapore's advanced biopharmaceutical manufacturing industry.
\nAs a trainee, you will gain hands-on experience, industry-relevant skills, and mentorship from experienced professionals in a world-leading biopharmaceutical environment.
\nThe programme is open to both fresh graduates and mid-career individuals who are passionate about developing a career in the biopharmaceutical manufacturing sector.
\nResponsibilities:
\nLearning Outcomes:
\nRequirements:
\nBenefits:
\n