Director

• Lead/Co-lead the planning, execution, and delivery of Veeva Clinical Operations technology and innovation programs
• Monitor and guide the execution of projects or components of larger initiatives, ensuring adherence to timelines, scope, budget, risk parameters, quality standards, and compliance requirements
• Create project plans with clearly defined deliverables, ensuring alignment across systems, data, processes, and stakeholders.
• Manage scope tracking, ensuring that acceptance criteria are well-defined and fulfilled.
• Support the definition of key performance indicators (KPIs) and metrics to assess project success.
• Facilitate retrospectives to identify improvement opportunities and support implementation of corrective actions.
• Lead risk management efforts by identifying potential risks with the project team and supporting the development of mitigation strategies, contingency plans, and escalation processes when necessary.
• Execute a professional Change Management and System Communication strategy , including: Comprehensive impact assessments for planned changes. Role-based communication plans tailored to stakeholder needs. Customized training materials designed to meet user expertise levels. Regular community engagements and meetings to align change initiatives.

Associate Director, Clinical Excellence

• Lead a team of diagnostic operations professionals to implement clinical biomarker and diagnostic plans for therapeutic programs in early and late-stage clinical development
• Line management, training, oversight, and retention of diagnostic operations professionals
• Maintain knowledge of the science, technology, portfolio, and strategy of R&D across Oncology and deliver high-quality diagnostic operations support
• Engage with and influence leaders and cross-functional stakeholders to develop diagnostic operational strategies by leveraging broad knowledge of biomarker technologies, diagnostic development, IVD expertise, and global diagnostic regulatory requirements
• Serve as a key strategic liaison with stakeholders across Clinical Operations, Central HBSM, Biobank, Data Management, Procurement, Regulatory, and Quality Assurance; work to improve cross-functional processes across GSK
• Contribute to the continued building of a framework within the Operations function focusing on growth and development of new and “innovative” ways to work with internal and external partners
• Lead functional process and system improvements to ensure operational excellence
• Proactively support developing and reviewing standard processes and templates
• Apply and adhere to ICH/GCP, HBS management best practices, regulatory guidelines, ethical guidelines, and technical and industry standards during all aspects of work, ensuring inspection readiness by ensuring preparedness and compliance; support team members in connection with inspections and audits
• Represent the Dx Planning & Execution department internally and externally in meetings and discussions as required, and ensure representation of the Dx Delivery team during cross-functional workstreams
• Set a positive and motivating work environment that encourages mutual respect, innovation, and accountability at all levels by role modelling the GSK values

Senior Director, Head of Diagnostic Execution

Vice President

• Own and deploy sterility assurance strategy, standards, and governance to ensure compliance to regulatory expectations.
• Lead cross-functional alignment and risk mitigation across Engineering, QA, and MSAT.
• Ensure contamination control strategy is standardized and embedded in QMS.
• Oversight of facility design and equipment reliability aligned with sterility assurance requirements.
• Lead cleaning validation, process control, and supplier qualification as it relates to sterility assurance standards.
• Ensure QMS integration, deviation management, and inspection readiness.
• Chair monthly governance forums and drive strategic decisions.
• Build capability through Communities of Practice.

Vice President – Sterility Assurance

Account Manager

• Drive product uptake by influencing prescribing decisions and establishing GSK therapies as preferred options for respiratory patients
• Develop and execute strategic account plans, collaborating with cross-functional teams to achieve objectives
• Build strong relationships and partnerships with NHS stakeholders, fostering collaboration and trust
• Communicate clinical data effectively, highlighting the benefits and NHS advantages of GSK therapies for respiratory management
• Enhance patient access by mapping service pathways, identifying and overcoming barriers, and supporting local access to treatments
• Monitor progress and adapt strategies using KPIs, data-driven insights, and an understanding of commissioning and reimbursement decisions

Key Account Manager – North East Yorkshire Lincolnshire

Chief Marketing Officer

• Collaborate with Global Medical, with other Global functions, with regions, and with Local Markets to support the development of Global Strategies that drive the brand revolution.
• Lead the delivery of Global marketing campaigns that drive HCPs- belief in unmet needs as well as conviction and motivation that our product can make a difference to people.
• Lead the delivery of HCPs support tools and enhance the user experience for providers and patients.
• Lead on our Nurse and MDT approach with customers
• Lead Global product Cx, AI & Digital Omnichannel to improve user experience throughout our customer journey.
• Engage and lead Regional and Local Market partners to ensure we are ambitious for our brand, and to drive pull-through of Global strategy and tactics across the ~30 countries where the brand is currently launched.
• Lead and manage global congress efforts, partnering closely with brand team and matrix partners
• Lead on external ambassador network and external engagement strategy
• Monitor performance metrics and use data-driven insights to optimize marketing activities
• Inspire and mentor a high-performing team, fostering innovation and collaboration, whilst providing them with opportunities to develop, grow and lead along the way.

Global Marketing Director

Full-stack Engineer

• Architect and build production-grade applications and data platforms
• Write production-grade code for full-stack applications using Python and modern frontend frameworks
• Build and maintain scalable REST APIs and microservices architectures
• Design application architectures and implement technical solutions
• Develop user interfaces and data visualization components
• Write comprehensive tests and ensure code quality
• Debug and optimize application performance
• Design and architect cloud-native applications and solutions on Azure
• Implement scalable, resilient, and cost-effective cloud architectures
• Optimize cloud resource utilization and performance
• Design for high availability, disaster recovery, and security
• Build and maintain data pipelines for large-scale data processing
• Implement ETL/ELT processes for diverse data sources
• Collaborate with data scientists to productionize ML models
• Evaluate and integrate new AI/ML technologies
• Participate in code reviews and knowledge sharing
• Contribute to technical discussions and solution designs

Senior Principal Software Engineer – R&D Tech

Manager

• Support forecasting activities for the US Specialty Business that guide commercial and supply decisions.
• Work closely with Marketing, Finance, Commercial Insights, Supply Chain and other teams.
• Establish, document, and maintain financial and manufacturing forecasts on a monthly cycle and annually revise Long-Range Forecast.
• Create SKU, patient and gross-sales level forecasts and monitor accuracy and bias using industry metrics for the US (including Puerto Rico).
• Run and present scenario modeling, identify risks and opportunities, and provide clear recommendations to multiple management levels.
• Partner with various teams to align assumptions and support launch planning.
• Ensure accuracy of forecasts through industry standard accuracy and bias metrics; identify corrective actions as appropriate.
• Translate market trends, competitor activity and customer insights into forecast drivers and actionable plans.
• Prepare timely responses for senior leadership requests and support quarterly financial processes as needed.
• In partnership with various stakeholders, develop, document, and maintain US Forecasts for priority pipeline assets from Phase 2 onward, including launch planning support.

Forecasting Manager

Clinical Research

• Lead data-driven country and site pre-selection and support final country selection for studies.
• Gather, review and analyse feasibility data from literature, databases, investigator registries and internal tools.
• Prepare and present feasibility documents including pre-selection proposals, questionnaires and kickoff meeting materials.
• Plan and chair feasibility meetings and coordinate cross-functional input from clinical operations, study delivery, regulatory and other stakeholders.
• Coach and support local study teams and central study leads in using feasibility tools and following the feasibility process.
• Hand over feasibility outputs to Study Start-Up teams to support timely submissions and critical path planning.

Feasibility Manager

Medical Director

• 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 understanding priority LOC (Local Operating Company) needs and success measures.
• Drives alignment across the internal ecosystem and with external partners to deliver Medical Plans that prioritize external impact above all else on time and on budget.
• Ensures team members and colleagues have a robust knowledge of the relevant and emerging clinical evidence by overseeing the creation and delivery of high-quality scientific materials for both internal and external use as well as implementing a global training and competency framework.

Senior Global Medical Director

• Establish, document, and maintain in-line products financial and manufacturing volume forecasts and annually revise Long-Range Forecast, in partnership with stakeholders.
• Maintain SKU level forecasts for General Medicines brands.
• Evaluate US market trends, competitor product landscape and competitive positioning as part of US Forecast development.
• Develop, document and present US Forecast, assumptions, opportunities, and risks, to multiple management levels.
• Ensure accuracy of forecasts through industry standard accuracy and bias metrics; identify corrective actions as appropriate.
• Support US financial submissions and quarterly earnings call, as needed.
• Collaborate and partner effectively with various stakeholders across the enterprise, including Marketing, Commercial Insight & Analytics and Managed Market teams, support senior management requests.

• Manage the team of associate directors, diagnostics.
• Team manager to deliver on the vision of equipping GSK to be a leader in oncology through Dx development driving the portfolio value
• Monitor and report projects progress, outcomes, KPIs eg delivery of Target Diagnostic Profile
• Remove barriers to Dx strategy development and implementation, collaborating cross functionally with clinical operations, external engagement, procurement, etc…
• Exhibits timely management and delivery of projects/work streams within agreed budget.
• Must be able to manage multiple projects and work streams across TAs and R&D, including assessment of workload and resourcing requirements to deliver the team’s objectives.
• Clearly and concisely report project progress and outcomes, coordinating with project management, finance and business operations
• Ensure learnings and best practices are shared and adopted for effective delivery
• Participate in the evaluation of advanced technologies for IVD and clinical biomarker development
• Keep a pulse on team execution and cross-functional ways of working with clinical, regulatory, operations, policy, BD and business unit colleagues and key leadership within project teams
• Provides frequent project status updates / reports related to Dx deliverables. Where applicable, accountable for implementing key organizational process improvement initiatives in daily activities

Director, Diagnostics

• Act as a single point of accountability in GSK for all aspects of a medicine in development globally from C2P2 to approval in first major markets.
• In addition to the overall leadership role, the MDL should provide key support to the Early Development Team (EDT) leading up to C2P2 to ensure smooth transfer of accountability and a successful C2P2 and transition from phase 1 to phase 2.
• In addition to the overall leadership role, the MDL should provide key support to the Medicines Commercialisation Team post-approval in first major markets ensuring that the MDT provide optimal support to both registration and lifecycle management.
• Selects members of the MDT, in consultation with the line leaders, and leads this multi-disciplinary matrix team; supports differentiated development for team members; owns the performance of MDT and partners with line managers to drive performance
• Establishes a compelling vision for the medicine; positions the medicine within the R&D strategy taking the competitive landscape into account; Translate GSK’s strategy into asset strategy and actionable plans for multiple areas or functions.
• Delivers differentiated medicines of value for patients, stakeholders and markets, through an evidence package that supports regulatory approval, market access, and product life cycle.
• Delivers the Medicine Development Strategy that is aligned with the R&D disease strategy, as well as the asset Medicine Vision and Medicine Profile.
• Prioritizes and maximizes the asset’s portfolio options including developing multiple indications.
• Makes clear evidence-based go / no go / accelerate decisions, based on whether the results fulfil the strategy set out for the medicine, and identify clear inflection points
• Embeds core processes including cost efficiency, adoption of new technology, risk identification & management, compliance with policy
• Identifies and aligns resources (people and financial), team objectives and strategies behind the vision to ensure successful project completion
• Proactively identifies unmet medical needs that could be addressed through line extensions
• Enhances patient focus by incorporating the voice of the patient into development plans.
• Promotes organizational reputation and drives asset value by engaging and negotiating with internal and external stakeholders
• Collaborates with other stakeholders but in particular EDLs and other MDLs to create strategies that support organizational vision; shares optimal ways of working and knowledge
• Ensures quality & compliance oversight in line with R&D expectations and project needs; assures quality of data and science
• Prioritizes and manages asset portfolio options to meet budget constraints.
• Model Values and Leadership Expectations internally and externally
• Asset single point of contact and spokesperson to senior management and senior boards (e.g., Chief Scientific Officer, Head of Development, Chief Medical Officer, President of Pharma, Development Review Board and Portfolio Investment Board) and other relevant internal governance committees and external Advisory Committees as needed.
• Increases visibility amongst the external communities (physicians, regulators, patients, payers), to bring medical solutions to patients with unmet medical needs, thereby enhancing reputation of GSK.
• MDL serves as the single accountable decision maker to resolve disputes among the MDT.
• The MDL should discuss any team misalignment/disputes with the Head of Development prior to rending a final decision.
• MDL is accountable for delivering and managing the asset resourcing plan.
• In addition, the MDL is accountable for managing the asset budget to the agreed variance.
• MDL is accountable for developing an ongoing patent strategy for the asset
• Partners with Business Development to facilitate diligence reviews, product positioning and/or alternative business strategies (e.g., public private partnerships, co-development) and internal review and decision-making processes in line with GSK governance procedures as well as use of appropriate alliance management mechanisms to ensure successful business transactions and relationships.

VP Medicine Development Leader – Oncology

Project Manager

• Manage CMC (Chemistry, Manufacturing and Controls) regulatory projects for a portfolio of devices (standalone and all types of drug-device combinations).
• Work closely with colleagues across supply, technical, quality and local operating companies.
• Lead CMC regulatory activities for an assigned portfolio of devices across global markets.
• Develop and implement CMC regulatory strategies and plans for lifecycle management and change control.
• Prepare variation dossiers and lead responses to questions from regulatory authorities.
• Coordinate and facilitate cross-functional CMC Regulatory Matrix teams and represent CMC in wider project teams.
• Ensure regulatory compliance is maintained and share best-practices and learnings within the CMC Regulatory teams and other impacted functions.
• Deliver CMC regulatory strategy to support major inspections (PAIs) with managerial support (occasionally).

Regulatory Project Manager – Devices

• Oversee projects deliverables and guide strategy and governance preparation for direct reports
• Facilitate and/or contribute to asset strategy and evidence strategy
• Own the single integrated plan that builds team commitment to shared goals
• Lead options planning, generate recommendations, alternatives, and trade-offs
• Identify opportunities to accelerate by challenging constraints that impact critical path
• Ensure rigor, consistency, and compliance in established systems
• Use strong facilitation skills to lead regular project team meetings
• Establish and sustain agreed-upon ways of working for effective team communication

Director, Pipeline Project Manager

Content Marketing Manager

• Ensure global promotional and non-promotional content meets the highest standards of quality, scientific accuracy, balance, and compliance
• Act as primary medical reviewer and/or approver for global materials
• Maintain deep scientific and therapeutic expertise on assigned products
• Provide feedback and recommendations for content created and/or reviewed by third-party vendors

Associate Director, Clinical Excellence

Senior Director, Head of Diagnostic Execution

Vice President – Sterility Assurance

Key Account Manager – North East Yorkshire Lincolnshire

Global Marketing Director

Senior Principal Software Engineer – R&D Tech

Forecasting Manager

Feasibility Manager

Senior Global Medical Director

Forecasting Manager

Director, Diagnostics

VP Medicine Development Leader – Oncology

Regulatory Project Manager – Devices

Director, Pipeline Project Manager

Associate Director, Content Approval – Vaccines