Compliance

• Contribute to the development and implementation of strategic advocacy plans
• Contribute to the execution of International regulatory policy, advocacy, and intelligence priorities
• Provide expert insights on targeted policy issues
• Build and maintain relationships with stakeholders
• Collaborate with internal teams to develop regulatory policy and advocacy strategies
• May lead global regulatory policy and advocacy strategy for select enterprise-level policy priorities

Manager, Global Regulatory Policy – International Markets

Content Manager

• قيادة استراتيجية المحتوى متعدد القنوات والتخطيط والتنفيذ لتحسين تجربة العملاء
• التعاون مع فرق التسويق، الطبية، الامتثال وآخرين لتحقيق أهداف العلامة التجارية
• ضمان التزام المحتوى بمعايير الجودة والتنظيم
• استخدام تحليلات المحتوى لقياس الأداء وتحديث المحتوى حسب الرؤى

Omnichannel Content Strategist

Director

• Own the product strategy for the operational heart of Development and CMO
• Empower R&D leadership to make high-stakes investment decisions
• Deliver tools that provide predictive analytics and actionable alerts
• Drive a cohesive strategy that innovates with AI, predictive analytics and automation
• Define and champion a 3-year transformative vision
• Lead, mentor, and develop a high-performing team of Product Owners and Product Designers
• Lead your team to act as catalysts for change
• Own the strategic curation and financial oversight of your product portfolio
• Serve as a strategic partner and trusted advisor
• Provide strategic oversight for the delivery of your product portfolio
• Ensure quality and compliance of your product portfolio

Senior Product Director, Performance Measurement and Improvement

Risk

• Lead data governance, standards and quality activities for Regulatory Information Management and Data Office (RIM&DO).
• Work with global teams across regulatory, IT, and business functions to ensure regulatory data is trusted, consistent and compliant.
• Define, implement and maintain data governance frameworks, standards and policies for regulatory information.
• Drive data quality programs, including data profiling, remediation plans and ongoing monitoring.
• Partner with Regulatory, IT and product teams to embed standards, and data governance and quality by design into systems, processes, and change controls.
• Lead cross-functional working groups to resolve data issues and improve end-to-end data flows.
• Develop and report meaningful metrics and dashboards to show data quality, risks and progress.

Associate Director, Data Governance, Standards & Quality

• Lead and manage a high-performing team of MSLs to drive field medical business performance
• Accountable for the direction and execution of strategic medical objectives and territory plans
• Collaborate with cross-functional business partners to enhance team effectiveness and drive overall team performance
• Ensure the team has a robust interface with external experts, healthcare professionals, and industry experts to gather insights and drive high quality scientific engagement
• Analyze and leverage scientific and performance data to provide actionable insights that support business development, product strategies, and clinical development strategies for Phase II through IV clinical plans
• Ensure team is well-trained with the latest scientific information and core industry compliance standards
• Lead MSL support of ViiV US sponsored and supported research in specific region

Senior Director, Field Medical, Southeast

• Mitigate access and reimbursement disruptions through education of office staff on payer coverage and policies, and acquisition pathways.
• Educate offices in navigating access and reimbursement challenges independently through the post-prescribing phase.
• Support complex access and reimbursement issues as needed.
• Identify and prioritize implementation barriers for removal at customer campuses.
• Develop strategic plans that include next actions, action owners and completion dates.
• Drive implementation barrier closure.
• Orchestrate coordinated plans across internal partners for aligned customers, built from a shared diagnosis.

Associate Director, Field Reimbursement

Content Marketing Manager

• Drive innovation and evolution through critical processes of the organization.
• Oversee the content review process and lead the content delivery team.
• Ensure accurate and efficient implementation of content platforms including AI tools.
• Interact with and influence teams such as Digital, Data and Tech, Promotional Content Governance Board, and others.
• Collaborate with stakeholders to identify and prioritize AI opportunities.
• Oversee the end-to-end lifecycle of AI projects, from ideation to deployment.
• Ensure compliance with relevant regulations and ethical guidelines.
• Communicate and present concepts to non-technical stakeholders.
• Develop and manage an annual budget, including SOWs, POs, and cross charges.
• Lead the Content Delivery team to ensure timelines and expectations are met.

Director, Promotional Review and Content Platforms

Communications

• Develop strong relationships between GSK and top-tier global and U.S. corporate media (e.g. New York Times, Wall Street Journal, Endpoints News etc.) to build understanding of and confidence in the company’s strategy, including our work to strengthen our pipeline of innovative medicines and vaccines, both via our in-house R&D efforts and business development activity.
• Develop and execute proactive strategies around key news flow regarding the company’s products and pipeline and be an active spokesperson on this news flow with key corporate media.
• Build a strong internal network to source ‘new’ stories – showcasing the company’s scientific innovation and expertise - of interest to corporate media, in support of the above objectives.
• Be a trusted counselor on a) the media, b) story generation and c) media handling to members of the Communication and Government Affairs (CGA) function Operating Committee, other GSK departments and senior executives up to and including the Chief Scientific Officer (CSO), as well as other members of the company’s R&D Leadership Team (RDLT) and Executive Committee (ExCom).
• This includes working closely with these executives, gaining their trust and briefing these executives ahead of (and staffing) media engagements.
• Anticipate issues where possible and produce issues management plans and materials for key corporate issues (e.g. litigation; restructuring; product safety).
• Handle crisis communications in a calm manner applying judgement and being trusted by executives in such situations.
• Handle out-of-hours calls often in pressurized circumstances.
• Handle highly confidential and price sensitive announcements/issues relating to business strategy including working with senior leaders and Corporate Secretariat as needed.
• Work closely with digital communications colleagues to maximize digital reach of announcements across channels and devise appropriate content.
• Support media strategy and communication plans for key corporate events such as external, media-sponsored medical and corporate conferences.
• Provide communications leadership and support to the US commercial business units to amplify and leverage milestones and campaigns.
• Actively contribute to CGA cross functional initiatives and/or team meetings.
• Bring external and market insights to the global corporate team.
• Drive media handling best practice through informal guidance and formal training of global CGA colleagues.

Director, External Communications

Affiliate Manager

• Provide Scientific Knowledge, Business Acumen, and Customer Engagement expertise to specialist customers in support of a GSK biologic product.
• To understand the reimbursement/distribution landscape for specialist customers and identify the appropriate resources (e. g. Payer Relations Managers, HUB, headquarter approved materials) to refer customers to appropriate resource for reimbursement and distribution choices, always working within GSK guidelines and values.
• Provide product educational programs/in-services to customers.
• Work within Compliance guidelines and GSK values always.
• Develop strategies and tactics to generate sales.
• Develop and implement strategies specific to each customer within an account (i.e., Rheumatologists, Nephrologists, nurses, mid-levels, business/office managers).
• Develop and maintain strong working relationships with Marketing, Payer Relations Managers (Market Access), Medical (MSLs), and other functions within GSK.
• Effectively manage allocated resources
• Provide outstanding customer service by responding to our customers' requests, inquiries and needs.

Business Partner – Specialty Account Specialist

Content Writer

• Lead strategy, planning, authoring and delivery of clinical documents across the asset lifecycle, including clinical study protocols, clinical sections of the IMPD/IND, investigator brochures, clinical study reports, briefing documents for regulatory authorities, Common Technical Document Summaries and Clinical Overview, and responses to regulatory authority questions.
• Own and drive asset-level medical writing strategy, ensuring alignment with development and regulatory objectives across regions
• Lead and coach multi-disciplinary matrix teams and external vendors to meet quality, timeline and budget expectations.
• Plan and deliver complex and accelerated global submissions, recommending innovative approaches to achieve ambitious timelines while proactively managing cross-functional interdependencies and risks.
• Create and maintain submission and document lifecycle plans.
• Advise teams on fit-for-purpose approaches and risk mitigation.
• Act as lead author or senior reviewer for complex submission documents and regulator queries, ensuring clear scientific positioning and compelling regulatory narratives.
• Define and recommend resourcing strategies for major projects, including optimal use of internal teams and external vendors
• Drive process and technology improvements that increase consistency, efficiency and document quality while constructively challenging the status quo.
• Mentor colleagues and build oncology medical writing capability through training, clear feedback and practical guidance, including contribution to training materials.

Director, Medical Writing Asset Lead – Oncology

• Chair the Global Integrated Medical Communication Teams (GIMCT) for assigned assets/therapeutic areas to drive the development of Integrated Medical Communication Plans (IMCP), inclusive of content, channel, and congress plans/tactics.
• Drive key asset deliverables including the Scientific Communication Platform (SCP), Scientific Narratives, Content and Channel plans, Congress Plans and all associated tactics.
• Serve as a key partner to therapeutic area medical leaders, global publications, R&D, Global Medical Team (GMT), and priority markets and regions.
• Collaborate with internal stakeholders on the development and execution of innovative tools for internal and external communication, including digital/social medical delivery.
• Drive timely execution of all deliverables within the IMCPs for assigned assets, ensuring they are scientifically accurate, evidence-based, and comply with relevant regulations, industry guidelines, and ethical standards.
• Accountable for aligning with key stakeholders and for the input of the IMCP framework and related engagement planning elements within the asset annual business planning process.
• Lead annual scope of work development with procurement for IMCP deliverables with agencies of record, and provide continuous oversight and feedback to drive effective collaboration and partnership.
• Ensure content development follows all relevant codes and system requirements (e.g. ABPI code of practice, GSK Code, and use of Content Lab), particularly with respect to the delivery of promotional versus non-promotional information.
• Participate in initiatives on Gen AI platforms being leveraged for content creation and personalization/adaptation to ensure broader scalability and use.
• Gather and share best practices across Global to ensure consistency, high standards, and excellence are maintained across the organization.
• Stay updated on advancements in scientific communications to ensure content approaches evolve with the external landscape.

Director, Global Content Design and Delivery – Oncology

• Influence changes to state laws and regulations within designated states to align with GSK's priorities and the pharmaceutical industry
• Engage patient advocacy groups, health professional societies, State Departments of Health and trade associations to support business unit needs at GSK
• Oversee those representing GSK’s interests before state governments
• Serve as the company’s registered lobbyist in both state legislatures and executive branch agencies
• Manage senior executive engagement with Government officials and key business groups
• Influence state legislation and regulation affecting GSK’s business interests in Oncology, Vaccines, Specialty, Respiratory and HIV with an emphasis on prevention policy
• Identify and establish annual legislative and policy objectives in coordination with Government Affairs management
• Develop and maintain a thorough working knowledge of existing state policies affecting GSK
• Manage GSK’s contract lobbyists or other consultants in key states as required
• Engage in legislative coalition-building and perform functions to ensure a legislative and regulatory environment that recognizes and rewards the value of innovative medicines
• Identify legislative and regulatory opportunities that support GSK’s business priorities

Director, State Government Relations

• Provides in-depth medical/scientific expertise in the safety evaluation and risk management of key GSK assets or in clinical development and/or the post-marketing setting.
• Ensures scientifically sound review and interpretation of data and management of safety issues and escalates safety issues identified through the safety review process to senior management and safety governance as appropriate.
• Makes recommendations for the further characterization, management, and communication of safety risks.
• Focus on efficiency and effectiveness to meet the needs of our Patients and HCPs.
• Supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally.

Senior Scientific Director, SERM

• Lead innovation in emerging diagnostic technologies, including ctDNA, computational pathology, advanced imaging techniques, and multi-modal biomarker platforms, to enhance patient stratification, therapeutic targeting, and mechanism-of-action insights.
• Develop and apply oncology foundational models and AI/ML analytical approaches to complex clinical, real-world and biomarker datasets, including high-dimensional data such as single-cell transcriptomics, spatial omics, proteomics, and cfDNA.
• Serve as a subject matter expert in application of analytical methods and emerging diagnostic technologies to enable biomarker discovery and diagnostic strategies to optimize patient selection, dose determination, and combination therapy approaches with a focus on antibody-drug conjugates (ADCs).
• Oversee the integration of oncology foundational models to inform translational medicine and clinical development strategies ensuring robust interpretation, practical implementation and timely communication across matrix teams.
• Collaborate with cross-functional teams, clinical development, CPMS (Clinical Pharmacology and Modeling Simulation), Diagnostic, Translational Research, and AI/ML teams, to evaluate and apply complementary data analytics approaches for meaningful insights into complex biology.
• Lead efforts to identify, evaluate, and implement emerging technology platforms to advance diagnostic innovation and support pipeline growth.
• Provide leadership and accountability for clear and timely communication of data analysis outputs, complex analytical principles, and models to diverse stakeholders, including senior leaders and non-technical partners.
• Champion the integration of biomarker and diagnostic strategies into clinical development plans, ensuring alignment with oncology research unit and translational medicine objectives
• Drive the application of computational pathology and AI-driven image analysis to enhance diagnostic capabilities and biomarker discovery in oncology programs.
• Support the evaluation of academic partnerships and external technology platforms, ensuring alignment with Oncology Translational Medicine goals and innovation priorities.
• Contribute to due diligence efforts for business development opportunities, leveraging expertise in advanced analytics and emerging diagnostic technologies.

Director, Integrative Sciences

Marketing

• Support and deliver against the overall mid- and long-term strategy for the brand.
• Develop, monitor and report on key metrics to assess the short-term performance of the brand across functions (KPIs, performance drivers, etc).
• Support the development of key leadership and governance presentations (MPR/IR, Forecast, etc.).
• Responsible for the overall brand budget (across functions), as well as forecast development, refinement, and tracking, in collaboration with finance, forecasting, and analytics.
• Lead Commercial Strategy Team for the brand, a matrix team of commercial leaders across finance, forecasting, insights & analytics, marketing, and market access.
• Strategic & Operational Planning.
• Strategic development of brand KPIs, measurement plans, and performance monitoring aligned to strategic imperatives and critical success factors.
• Development of leadership and governance documents (i.e. Monthly Performance Review (MPR)/Monthly Operational Review (OPR), Investor Relations (IR), launch readiness reviews (LRRs), etc.).
• Serve as marketing lead / point of contacts for Insights & Analytics, Competitive Intelligence, Forecasting and Supply.
• Strategic LCM (Lifecycle Management) Strategy for a multi-indication product, including identifying current & future opportunities and prioritization of investment by indication as appropriate.
• Lead assessment of market development and key commercial opportunities to optimize launch planning.
• Identify and integrate novel data sources (biomarker, lab, claims, RWE, etc.) to enhance marketing strategies.