Account Specialist

• Support specialist healthcare providers across the assigned territory
• Build and maintain relationships with pulmonologists, allergists, nurse specialists and practice managers
• Deliver clear, evidence-based clinical education and support to specialist teams
• Identify reimbursement and distribution needs and connect customers with appropriate support resources
• Develop tailored account plans and tactics to drive patient access and service
• Work with market access, medical affairs and marketing partners
• Adhere to compliance and ethical guidelines in customer interactions
• Travel regularly within the territory and occasionally beyond it
• Drive as an essential function of the role

Specialty Account Specialist, Respiratory

Communications

• Lead integrated communications and patient advocacy strategies across GSK's US Oncology portfolio
• Manage a team of communications and advocacy professionals while aligning cross-functional and global partners
• Elevate patient perspectives, strengthen advocacy organization partnerships, and inform business and policy decisions
• Develop and execute plans supporting priority brands, launch assets, pipeline programs, clinical data milestones, regulatory events, business development initiatives, and scientific congresses
• Partner with Commercial, Medical, Market Access, Policy, and Government Affairs teams on launch readiness, disease awareness, access objectives, and stakeholder engagement
• Deliver data-driven, science-based engagement strategies for patients, healthcare professionals, caregivers, advocacy organizations, media, and other stakeholders
• Secure recognition and visibility for oncology data, innovation, scientific leadership, business milestones, and patient impact
• Own external and reputational issues management for the oncology portfolio
• Coordinate strategic responses that protect and strengthen GSK's reputation
• Lead communications and advocacy strategies supporting business performance, transformation, culture, and employee engagement
• Advise the Head of US Oncology and the Oncology Leadership Team
• Serve as a trusted advisor and thought partner to Oncology leaders and the broader US Communications & Government Affairs organization
• Measure impact using outcomes, performance indicators, data, analytics, stakeholder insights, and emerging technologies
• Manage and develop team members and agency partners while ensuring compliance with GSK standards and policies

Senior Director, US Oncology Product, Pipeline, Patient Communications & Advocacy

Account Manager

• Lead GSK’s global Nature strategy, including vision, objectives and roadmap
• Oversee Nature initiatives across key business areas with priorities, KPIs, governance and business ownership
• Lead the Nature & Partnerships team through coaching, line leadership and succession planning
• Partner with Supply Chain, R&D, Procurement, Real Estate, EHS and Finance to embed nature considerations into decisions
• Build external partnerships to support strategy delivery and strengthen GSK’s influence
• Support Nature-related governance and reporting into executive forums
• Track external policy, regulatory, standards and investor expectations on Nature
• Represent GSK’s Nature agenda internally and externally in stakeholder engagement, communications and ESG disclosures
• Drive continuous improvement and innovation in Nature approaches
• Manage Nature programme budgets and influence related investment decisions
• Deliver Nature strategy and programmes across GSK’s regions and business units

Head of Nature and Partnerships

Medical Director

• Develop and own Project Charters and Scope Statements defining CMT objectives, scope, stakeholders, and success criteria
• Lead Project Kickoff Decks and align teams at initiation
• Build and maintain Stakeholder Registers, Communication Plans, and Governance Calendars
• Create and maintain CMT plans translating CDP milestones into schedules, dependencies, and critical-path activities
• Own RACI Matrices and Governance Frameworks
• Maintain risk, issue, dependency, requirements, deliverables, decision, action-item, milestone, change, and compliance logs
• Produce recurring Status Reports, Project Dashboards, Stakeholder Communication Summaries, and Executive Summary Reports
• Develop Quality/Test Plans and Compliance Checklists
• Deliver Lessons Learned/Closeout Reports and Post-Implementation Reviews
• Facilitate monthly governance and review meetings, including agendas, actions, and minutes
• Ensure rigor, consistency, compliance, and high-quality data in PM systems and templates
• Build relationships with functional leads and stakeholders and support conflict resolution
• Escalate risks and issues to leadership as required
• Promote GSK’s Code and values and seek diverse perspectives

Associate Director, Clinical Development Project Manager – Oncology

Scientist

• Perform targeted and non-targeted trace analysis of small and large molecules using mass spectrometry
• Develop sample preparation approaches and strengthen analytical capability within the laboratory
• Develop, optimise, validate or verify LC-MS and GC-MS methods for project needs
• Assess extractables and leachables risk and deliver practical risk mitigation strategies for individual projects
• Lead analytical work from sample preparation through data interpretation, reporting and project recommendations
• Contribute to regulatory submissions
• Oversee agreed work packages delivered by contract research organisations
• Support trace analysis for mutagenic impurity and elemental impurity control in pharmaceutical samples
• Contribute to analytical projects from sample preparation through final report
• Lead development of trace-level control strategies for individual projects

Trace Analysis and E&L Scientist

Medical Advisor

• Provide high-standard scientific and technical expertise for local medical information
• Interact with Key External Experts and Key Opinion Leaders
• Provide medical and scientific input for regional business strategy
• Develop and sustain networks with appropriate Health Care Practitioners
• Plan, facilitate, and conduct CMEs, symposia, trainings, workshops, scientific meetings, speaker tours, and product-specific campaigns
• Deliver consistent on-label scientific presentations at medical education meetings
• Support Scientific Engagement activities according to Medical Plans
• Develop expertise in Hepatology and support activities related to GSK brands
• Maintain current knowledge of Hepatology, GSK molecules, and product information for on-label communications
• Support feasibility assessments of research sites and develop concept notes, proposals, budgets, data-collection tools, and monitoring tools for field studies
• Provide medical input into brand strategy development and execution
• Support the Named Safety Contact in strengthening Hepatology pharmacovigilance

Area Medical Advisor, Specialty, Hepatology

Product Manager

• Manage and deliver the solid oral, liquid, sterile and topical dosage product portfolio
• Own and provide technical leadership for products or product families at local and/or global level
• Serve as Technical Product Owner throughout the product lifecycle
• Lead new product introductions, technology transfers, scale-up, validation and handover to manufacturing sites and contract partners
• Own product technical knowledge, performance monitoring, process capability, robustness and continuous process verification
• Assess and approve technical changes using risk management tools
• Maintain current product control strategies and mitigation plans
• Lead investigations and root-cause analysis for deviations, complaints, CAPAs, audit findings and complex product-performance issues
• Prepare and review risk assessments, specifications, validation reports, qualification documents and periodic product reviews
• Support PLM lead with implementation and sustainability
• Support statistical analysis and statistical capability building in ES India
• Collaborate with Quality, Operations, Engineering, R&D, suppliers and global sites
• Coach teams and strengthen technical and statistical capabilities

MSAT Product Owner

Clinical Operations

• Lead and support operational strategy and delivery for assigned late phase development streams, ensuring alignment with the clinical development plan.
• Coordinate cross-functional inputs from clinical, biostatistics, safety, clinical supplies and vendors to meet timelines and quality expectations.
• Represent DevOps at EDT/MDT.
• Contribute to protocol development, operational feasibility assessments and resourcing decisions, including insourcing versus outsourcing recommendations.
• Maintain inspection readiness and quality oversight, supporting risk management, mitigation plans and serious breach escalation when needed.
• Provide operational input for regulatory deliverables and governance forums, including scenario modelling and budget forecasting for clinical activities.
• Act as a point of contact for stakeholders and vendors to ensure consistent execution across studies and sub-projects.

Associate Director, Associate Clinical Operations Asset Lead

Vice President

• Lead, coach, and develop a regional team of Strategic Oncology Account Directors
• Set expectations, provide actionable feedback, and build account leadership skills
• Support in-field engagement and maintain relationships with C/D-Suite Population Based Decision Makers across academic cancer centers and community oncology networks
• Direct development and execution of GSK’s go-to-market model across community oncology, health system accounts, and leading cancer centers
• Partner with Market Access, Pricing & Contracting, Medical, oncology business unit, and GSK account teams
• Negotiate and pull through contract agreements aligned to access and customer strategies
• Integrate oncology brand strategy, access, and system-level initiatives to realize business opportunities
• Deliver regional strategic plans and achieve performance goals using KPIs including patient access, formulary status, pathway inclusion, and clinically appropriate use
• Conduct internal business strategy discussions and performance reviews
• Build connectivity across US oncology brand teams, Market Access, Medical, and cross-functional partners
• Use marketing research, market intelligence, clinical messaging, and account insights to inform strategies
• Support account-based campaigns, tools, and resources across key accounts
• Ensure adherence to GSK policies, Write Right principles, and compliance standards
• Represent GSK at sponsored industry events
• Role-model GSK’s values and foster trust, accountability, and continuous development

Field Vice President, Market Access Oncology, Strategic Accounts

• Lead the US Medical Communication Strategy and Plan for one or more Vaccines assets
• Provide a strong US voice on the Global Integrated Medical Content Team and share accountability for global medical content
• Develop, execute, and regularly update the US Medical Integrated Scientific Communication Plan
• Ensure the Scientific Narrative is relevant to the US market and aligned with evidence generation plans, medicine strategy, and the US marketplace
• Lead Medical Communication Strategy and objectives, ensuring content is fit-for-purpose for scientific exchange across formats
• Lead development and delivery of omni-channel customer experiences and medical communications with the US Medical Digital and Tech team
• Develop key performance indicators, measure impact, and optimize customer experience using data and analytics with the US Medical Analytics team
• Develop and maintain the medical curriculum and scientific training plan for Vaccine medical staff, including new hires
• Provide Medical Business Leadership for vaccine congresses, including customer experience, medical communications plans, and associated activities
• Apply medical governance in alignment with relevant GSK policies and procedures
• Collaborate with medical experts and cross-functional teams including Global Medical, Field Medical, Clinical Development, and Commercial

Director, Medical Communications and Scientific Training

Compliance

• Lead planning, compilation and delivery of regulatory submission dossiers for lifecycle activities
• Coordinate with global submission teams, clinical, CMC, quality, publishing and local regulatory partners
• Plan, compile and deliver electronic and paper regulatory dossiers within agreed timelines
• Coordinate cross-functional inputs from clinical, CMC, quality, safety and commercial colleagues
• Build, validate and quality-check electronic submission packages
• Resolve technical validation issues
• Maintain submission trackers, version control and milestone plans for transparency and audit readiness
• Prepare responses to regulatory authority questions
• Support regulatory meetings when required
• Identify and implement process improvements
• Coach colleagues and share best practice
• Help improve patient access through regulatory excellence

Regulatory Submission Lead

Data Analyst

• Complete a one-year industrial placement beginning in July 2027
• Work on live projects or assignments with genuine impact in GSK’s biopharmaceutical operations
• Support pharmaceutical manufacturing through process monitoring, performance analysis, process mapping, equipment evaluation, continuous improvement, deviation investigation, risk assessment, and root cause analysis
• Support business analytics and KPI improvement at the Worthing site
• Engage site teams in Digital, Data & Analytics culture and support GSK Production System rollout
• Work with production areas to execute improvement plans
• Develop digital solutions using AI, Power BI, Power Apps, and machine learning
• Work with APIs, data pipelines, integration patterns, data governance, reproducibility, documentation, and operational support in regulated R&D environments
• Contribute to predictive modelling, compound profiling, target identification, or translational biomarker discovery projects
• Develop automated data processes, datasets, dashboards, and visualisations
• Apply Python, R, SAS, Power BI, and Microsoft Power Platform
• Analyse product and process data to identify trends and support root-cause analysis
• Translate business and scientific requirements into practical data solutions
• Collaborate with manufacturing, quality, technical, digital, engineering, and multidisciplinary teams
• Support data integrity, GMP, validation, Agile working, continuous improvement, and sustainable zero-waste and zero-defect initiatives

Data Analyst, Industrial Placement

Director

• Integrate technical attributes, patient and user needs, business requirements, competitive landscape and technologies for drug-device combination products
• Support development efforts to improve the probability of technical success of development programs
• Collaborate with Discovery, Clinical, Commercial, Quality, Manufacturing Science and Technology, Regulatory and Drug Product Development teams
• Develop on-target, patient-centric drug-device combination products and ensure integrated product development
• Engage early to understand technical requirements and challenges, develop product concepts, and outline investment requirements, tradeoffs and risks
• Identify technical risks and lead mitigation using testing and modelling to support device selection
• Plan and execute engineering studies, device characterization, design verification and validation
• Author and review key technical documentation and regulatory submissions
• Support industrialization and technology transfer of devices to manufacturing sites
• Provide process development support, design for manufacturability and resolution of device-related challenges
• Monitor industry trends and collaborate with academia, government organizations and professional consortiums associated with drug-device combination products

Associate Director – Concept Development and Delivery

Procurement

• Lead end-to-end category and sourcing strategies for outsourced large-molecule drug substance and drug product manufacturing services
• Run complex sourcing activities and negotiate contracts, including master service agreements, statements of work, pricing arrangements and long-term capacity agreements
• Manage strategic relationships with contract development and manufacturing organisations and other critical external partners
• Work across Procurement, External Manufacturing Operations, R&D, Technical, Supply Chain, Quality, Finance, Legal and product teams
• Support new product introductions, technology transfers, capacity expansion, supplier transitions and supply-continuity activities
• Balance value, quality, service, resilience, innovation and risk in commercial and supplier decisions
• Establish credibility with business and supplier stakeholders and progress sourcing and contracting activity at pace
• Turn business requirements into procurement strategies, lead negotiations and make well-reasoned decisions

Senior Manager – External Manufacturing Procurement

Executive

• Lead commercial growth and customer engagement across an assigned territory in India
• Build and maintain trusted relationships with healthcare professionals, hospital teams and institutional stakeholders
• Create and deliver territory business plans to meet commercial targets and support improved patient outcomes
• Conduct professional visits and educational meetings to share clear, evidence-based information
• Gather market and customer feedback and use insights to shape local plans and improve execution
• Work with colleagues across functions to solve customer needs and ensure high-quality delivery
• Ensure all activities comply with company policies, quality standards and local regulations