Account Manager

• Build partnerships with large-organized customers, incl. HSs, Public Awardees & FQHCs and key decision-makers
• Identify the customer’s objectives/goals and how vaccination efforts can help support
• Develop robust customer-specific and area Business Plans leading to Good Selling Outcomes/GSO
• Navigate complex organizational structures to identify clinical operational and financial influencers
• Work closely with Public Sector decision makers to advance immunization efforts and address local policy shifts
• Represent needs to Field and HQ leadership for timely support

Vaccine Account Manager

Medical Director

• 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
• Makes recommendations for the further characterization, management, and communication of safety risks.
• Supporting the pharmacovigilance and benefit-risk management of the assigned portfolio of GSK global assets to ensure Patient Safety globally.

Operations

• Lead operational quality across all GSK vaccines manufacturing sites to ensure supply continuity and patient safety
• Set site-level quality priorities, metrics and governance with clear owners and deadlines
• Oversee investigations, root cause analysis and robust corrective and preventive actions
• Deliver simplification and continuous improvement projects that improve quality, speed and cost
• Grow capability through coaching, succession planning and inclusive leadership of quality teams
• Partner with cross-functional teams to support inspections, transfers and new investments
• Translate global and regional quality strategy into clear operational plans for Belgium sites
• Run quality governance meetings and provide timely, transparent updates to senior stakeholders
• Ensure compliance with good manufacturing practice, data integrity expectations and local laws
• Monitor quality performance and act decisively to close gaps and mitigate risks to supply
• Provide oversight for commissioning, qualification and transfer activities at sites and partners
• Promote digital and data-led improvements to make quality processes simpler and more reliable

Senior Director, Quality Operations – Vaccines

Research Scientist

• Generate large-scale analysis outputs
• Implement state-of-the-art tools for dynamically analysing, interpreting, and visualizing genetic and genomic data
• Evaluate, improve, test, and develop production implementations of best-in-class methods for analysis of genetics and genomics data
• Collaborate with partners across TSci, in experimental Target Discovery, and in GSK disease area Research Units
• Stay informed about recent research in the field and considering its potential for application within GSK
• Contribute to a culture of innovation, quality, and willingness to learn and improve.

Principal Scientist, Genomic Technologies

Compliance

• Lead CMC regulatory strategy for investigational and early commercial biological products across global teams.
• Understand, interpret and advise on regulations, guidelines, procedures, policies and strategies relating to development, registration and manufacturing of biological products.
• Serve as a key strategic partner representing Global CMC Regulatory on cross-functional networks and matrix teams.
• Own submission content and ensure regulatory requirements for clinical trials, product release and stability are in place.
• Participate in corporate evaluation and provide CMC regulatory support/advice to in-licensing and divestment projects.
• Identify regulatory risks and propose clear mitigation plans to senior leadership.
• Support major inspections and quality incidents by producing regulatory strategy and managing regulatory interactions.
• Mentor and develop regulatory colleagues, may have direct line management responsibilities as per business needs.
• Has accountability for information submitted in marketing applications to meet regional requirements.

Director, CMC Regulatory Affairs

Artificial Intelligence

• Manage stakeholder engagement: Proactively interact with stakeholders, line and middle management, staff and external contacts on a functional and tactical level.
• Tactically identify high impact opportunities for hybrid AI/ML-pharmacometrics approaches on projects.
• Execute portfolio projects: Apply AI/ML and hybrid AI/ML-pharmacometrics approaches to deliver analyses that inform drug development decisions (dose, regimen, endpoint, population, trial design).
• Work cross-functionally: Collaborate with CPMS leads, QSP modellers, statisticians, and digital/imaging experts to integrate AI/ML analyses with existing modelling frameworks.
• Contribute to our capabilities: Engage with academic groups and external vendors supporting joint internal-external projects and remaining abreast of cutting-edge methods.
• Identify best practices, trends, learnings, etc from internal and external sources and disseminate.
• Drive awareness: Deliver training, seminars, and internal communications to increase literacy in AI/ML-pharmacometrics across CPQM and RIIRU.
• Have external influence: Conference presentations, posters, and publications in scientific journals to represent GSK’s impact in AI/ML for drug development.

Director – MIDD AI/ML Scientist

• Create a strong link between Clinical Development and Pre-clinical/ Discovery teams
• Engage in medical dialogues with relevant scientific and medical leaders
• Lead clinical data generation activities
• Manage effective relationships with Key External Experts
• Oversee development and execution of early phase interventional clinical trials for patients with prostate cancer
• Ensure high quality protocol development and timely delivery of clinical trials
• Interpret and summarize study results
• Review/monitor safety data in collaboration with pharmacovigilance group
• Participate in authoring of clinical study reports and regulatory documents
• Network extensively to develop long-term strategic partnerships with thought leaders

Early Clinical Development Medical Director, Oncology

Director

• Responsible for setting the vision, defining the Business Unit strategy for Speciality business
• Leads the BU team members and cross-functional team to deliver a superior patient & customer experience
• Develops effective sales & marketing strategies to ensure successful performance
• Fully accountable for the local business, including currently marketed products and any future products
• Establishes a financial plan including units, sales and expenses in alignment with overall financial planning process

Specialty Business Unit Director

Manager

• Lead end-to-end root cause investigations for cross-functional and high-risk issues, using structured methods to reach evidence-based conclusions
• Coach and support colleagues on investigation tools, risk assessment and SMART CAPA design
• Oversees the CAPA closure and effectiveness implementation
• Partner with process owners and stakeholders to simplify workflows, reduce recurrence and improve issue management practices
• Facilitate the management review and oversight by proactively monitoring signals and business performance
• Assess Issues for criticality and Serious Breaches

Senior Manager, RCI & CAPA

• Oversee regulatory strategy globally for the RI&I portfolio
• Act as a direct link between Regulatory Affairs and all RI&I R&D stakeholders
• Ensure appropriate regulatory compliance in the conduct of global development programs
• Drive sound regulatory practices integrated into pre-clinical, clinical, and technical submissions
• Contribute to the creation and implementation of development plans to maximize successful regulatory applications
• Develop and maintain relationships with FDA, EMA, PMDA, CFDA, and other key international regulatory agencies
• Provide leadership to assure appropriate regulatory compliance in clinical trials

Vice President, Global Regulatory Affairs Strategy

Strategy

• Lead the Vaccines Product Quality Strategy organization and shape how quality supports global supply and patient impact
• Work with leaders across Quality, R&D, Supply and Commercial to set strategy and drive risk-based decisions
• Define and deploy a clear product quality strategy for Vaccines that aligns with global quality objectives
• Lead enterprise-level product quality risk management and governance, including escalations and strategic reviews
• Partner with cross-functional leaders to prioritise quality investments, deliverables and continuous improvement programmes
• Oversee critical quality metrics, audits and regulatory readiness to maintain supply and compliance
• Sponsor digital and data initiatives that simplify quality processes and improve decision making
• Build capability and coach teams to embed a proactive, predict-and-prevent quality mindset
• Manage quality governance forums and deliver regular, transparent updates to senior stakeholders
• Lead root cause investigations and ensure robust corrective and preventive actions are implemented
• Support regulatory inspections and responses, working with operational teams and external authorities

Senior Director – Product Quality Strategy

• Work to generate, validate, and integrate multimodal generative AIML models for the de novo design and multi-objective optimization of tool and therapeutic biologics
• Build and exploit agent-orchestrated, integrated Design-Make-Test cycles with automated experimental platforms generating quality data at scale needed for project-specific and foundational models
• Innovate, develop, and apply predictive models for protein design and developability engineering
• Collaborate with external groups to further develop protein engineering computational methods

Associate Director – Scientific Leader, Protein Design and Informatics

• Lead the global labelling process for GSK’s development portfolio through early lifecycle stages.
• Ensure regulatory requirements related to product information and submission strategies are met, proactively resolving issues across therapy areas.
• Provide strategic direction for labelling governance and represent GSK in global labelling committees and industry events.
• Advise senior management and regulatory teams on product labelling policies, standards, and compliance.
• Manage and motivate the Strategic Labelling team (including team leaders and their teams), fostering collaboration and alignment with GSK’s principles.
• Represent GSK in industry groups and during internal and external regulatory inspections or audits related to labelling governance and processes.

Executive Director – Strategic Labelling

• Serve as a key thought leader in digital transformation and HCP engagement.
• Ensure that cost‑effective, innovative digital solutions align with each Therapeutic Area’s priorities.
• Drive leadership and innovation across digital engagement, automation, business planning, and next‑generation tools, including AI.
• Support all medical affairs functions—from scientific communications and field enablement to digital execution, data generation, and congress activities.
• Act as a trusted advisor operating within a multi-stakeholder sphere of influence.
• Manage complex relationships and dependencies across internal teams and service partners.

Director of Medical Affairs, Digital, Data & Technology

• Support the Global Medical Portfolio and Asset Strategy Leads in the development and timely execution of practice changing Global Medical Affairs Plans (MAP) and Integrated Evidence plans (IEP) in partnership with key stakeholders through the GMAT and IET.
• Thinks globally, while deeply understands priority LOC (Local Operating Company) needs and success measures.
• This is accomplished through extensive partnership and collaboration with LOC teams to understand landscape, market value drivers, unmet medical needs and timelines for deliverables required for their success.
• Partners across the internal ecosystem and with external partners to deliver Medical Plans that prioritize external impact above all else on time and on budget.
• Leveraging insights and learnings, inputs into the design of clinical trials and development plans to optimize the positive impact for patients.
• Drives excellence in scientific engagement by developing a strong collaborative network of global external experts (HCPs, patients, payors and regulators) to be engaged in advice seeking activities and appropriate initiatives to advance clinical care and patient outcomes in partnership with the LOC Medical teams where those experts reside.
• Ensures colleagues have a robust knowledge of the relevant and emerging clinical evidence, supporting their training by partnering on the creation and delivery of high-quality scientific materials for both internal and external use.
• Partner with Global Product Strategy, Market Access, and core country teams to support/advise on core claims and material review.
• Ensure appropriate medical governance oversight including management of product-related issues with potential impact on patient safety and of risk assessment and mitigation plan associated with deliverables/strategies.
• Development of deep subject matter expertise on the product and therapy area as well as the ability to drive proactive strategic planning.
• Drive a culture and delivery mindset of future ready innovation which supports faster and specific solutions for patients.
• Engages across the ecosystem, including R&D, Evidence Generation, Global Product Strategy, and country teams to support identification and prioritization of evidence generation needs to close gaps and support the optimization of clinical care all aligned via the IEP.
• Review GSK-sponsored and investigator-sponsored study (ISS) proposals to assess their strategic alignment and scientific merit, in liaison with R&D, safety, biostats and other experts.
• Leads the creation and implementation of an integrated external medical communications plan which is optimized to deliver external impact and considers all channels (including publications and congresses) and key market needs.
• Develop and communicate the strategic publications plan in collaboration with the Publications Lead and other stakeholders.