Account Manager

• Manage a defined territory in Charleston, SC to build strong, trusted partnerships with oncology care teams.
• Create and execute territory business plans that improve patient access and deliver measurable results.
• Work closely with cross-functional colleagues including medical affairs, market access, and commercial operations.
• Build and maintain relationships with oncologists, specialty pharmacists, nurse navigators, and institutional accounts in Charleston, SC.
• Identify key prescribers and accounts and apply resources to support their needs and priorities.
• Use customer insights and data to prioritize actions, set goals, and measure performance.
• Support launches and local promotional activities through coordinated, compliant field programs.

Oncology Account Manager – Hematology

Medical Director

• Develop US-specific medical strategy, ensuring alignment with global asset strategy and US customer needs.
• Provide strategic oversight of US tactical plans and ensure alignment with therapeutic portfolio and disease-area strategies.
• Engage external communities to advance scientific understanding, appropriate use of medicines, disease management, and patient care.
• Coordinate external expert engagement with US Medical Science Liaisons (MSL) and Global Medical Asset Leader (GMAL).
• Support creation of medical materials for scientific engagement.
• Review, synthesize, and analyze clinical trial data, translating it into actionable plans.
• Develop strategies for Medical Advisory Board, Expert Panel meetings, Medical Grants, and Medical Publications.
• Support Medical Information team on FAQs and medical information responses.

Vaccines Medical Director – Herpes Zoster

Insurance

• Provide hands-on microbiology support for sterile operations, including aseptic processing, environmental monitoring, and gowning qualifications.
• Lead investigations of unexpected microbiological results and drive corrective actions with clear root cause and risk assessment.
• Perform and review routine microbiological testing: bioburden, sterility, endotoxin, microbial identifications, and water testing.
• Develop, revise, and approve microbiological methods, SOPs, and sampling plans that support product release and stability programs.
• Partner with manufacturing, quality, and development teams to define and implement contamination control and sterility assurance strategies.
• Support validation activities, method transfers, and evaluation of rapid microbiological technologies.

Senior Scientist, Microbiology – Sterility Assurance

Director

• Deliver a single, reconciled, and trusted view of brand performance, drivers, risks, and outlook across specialty and anti-infective brands
• Own product analytics priorities aligned to brand strategy, launch plans, and the annual operating plan
• Translate complex data into clear, executive-ready insights that inform leadership decision-making and resource allocation
• Lead Insights Development teams aligned to promoted specialty and anti-infective brands
• Ensure lifecycle-based scaling of analytics support across pre-launch, launch, and early growth phases
• Oversee field analytics including targeting, incentive compensation (IC) reporting, and launch execution tracking
• Drive marketing and omnichannel analytics to inform investment decisions and optimize launch effectiveness
• Oversee brand-specific data environment configuration and data operations to support launch and in-market needs
• Lead a high-performing I&A team aligned to business priorities
• Serve as the primary I&A thought partner to BU leadership for specialty and anti-infective brands.

Senior Director, Pipeline Business Insights & Analytics

Engineer

• Definition of schemas and data models of scientific information required for the creation of value adding data products.
• This includes accountability for the quality control and mapping specifications to be industrialized by data engineering and maintained in platform provisioned tooling.
• Accountable for the quality control (through validation and verification) of mapping specifications to be industrialized by data engineering and maintained in platform provisioned tooling – e.g., models, schemas, controlled vocab.
• Working with Product managers/engineers confidently convert business need into defined deliverable business requirements to enable the integration of large-scale biology data to predict, model, and stabilize therapeutically relevant protein complex and antigen conformations for drug and vaccine discovery.
• Collaborate with external groups to align GSK data standards with industry/ academic ontologies ensuring that data standards are defined with usage/analytics in mind.
• Support effective ingestion of data by GSK through understanding the entry requirements required by platform engineering teams and ensuring that the “barrier for entry” is met e.g. Scientific information has the appropriate metadata to be indexed, structured, integrated and standardised as needed.
• Provides bespoke subject matter expertise for R&D data to translate deep science into data for actionable insights
• Champion data lineage, data quality, and FAIR data principles across the Onyx platform, working with engineering and product teams to embed governance and quality frameworks into data pipelines
• Contribute to and maintain documentation of data standards, ontology decisions, and mapping rationale to support organizational knowledge transfer and auditability
• Support self-service data enablement by ensuring metadata and knowledge products are accessible, well-documented, and usable by scientists and analysts without requiring bespoke engineering support

Senior Scientific Knowledge Engineer

• Defining and executing model-based development strategies for oncology projects
• Planning, conducting and reporting exposure-response analysis, simulation-based trial design and dose selection
• Applying innovative methods such as drug-disease modeling, longitudinal exposure-response analysis
• Presenting strategy and defending outcome of model-based approaches to internal governance boards and regulatory agencies
• Write or review clinical pharmacology components of regulatory documents and responses

Director, Oncology Clinical Pharmacology, Modeling and Simulation

Data Engineer

• Designs, builds, and operates data tools, services, workflows, etc that deliver high value through the solution to key business problems by leveraging modern data engineering tools (e.g. Spark, Kafka, Storm, …) and orchestration tools (e.g. Google Workflow, AirFlow Composer)
• Confidently optimizes design and execution of complex solutions in data ingestion and data transformation
• Enables data products optimized for AI/ML and GenAI workloads—high throughput, observable, feature-ready and governed
• Produces well-engineered software, including appropriate automated test suites, technical documentation, and operational strategy
• Implements modular, reusable components and microservices that accelerate development and reduce operational overhead
• Provides input into the roadmaps of upstream teams (e.g. Data Platforms, DataOps, DevOps) to help improve the overall program of work
• Ensure consistent application of platform abstractions to ensure quality and consistency with respect to logging and lineage
• Fully versed in coding best practices and ways of working, and participates in code reviews and partnering to improve the team’s standards
• Adhere to QMS framework and CI/CD best practices and helps to guide improvements to them that improve ways of working
• Provides technical leadership, code reviews, architectural guidance, and mentorship to junior engineers and serves as an escalation point for complex operational issues across pipeline and data services.

Senior Data Engineer

• Engage with a highly significant group of customers on a peer-to-peer level
• Engage with PCN/Federations/ICB stakeholders within the Vaccines and Respiratory environment
• Accelerate effective implementation of a Vaccines National Immunisation Programme across the NHS system through engagement with ICB/Federation/PCN Stakeholders
• Implement COPD QIP led initiatives through collaboration with various Pharmacists and Directors
• Demonstrate a high level of omni-channel selling skills to ensure medicines are prescribed and initiated in appropriate patients
• Work collaboratively with regional colleagues and be accountable for the achievement of sales growth and delivery of activity targets across a defined group of customers

Pharmacist Account Manager – Midlands

Compliance

• Manages multiple CMC (Chemistry, Manufacturing and Control) renewals assignments for Pharma and Vaccines products
• Defines and agrees on regulatory strategy
• Completes data assessment to ensure CMC dossier is authored in compliance
• Identifies risks associated with submission data and information packages
• Escalates issues with line manager
• Understands regulations, guidelines, procedures and policies relating to registration and manufacturing of pharmaceutical products
• Identifies improvement opportunities for regulatory processes, policies, and systems
• Effectively communicates in a digital context, including virtual meetings and digital platforms
• Works with colleagues in Global Manufacturing & Supply and GSK Local Operating Companies in markets worldwide
• Monitors regulatory intelligence and acts proactively on identified changes

Regulatory Specialist

• Safeguard the quality, consistency, and reliability of Individual Human Data (IHD)
• Ensure critical R&D data is accurate, standardized, traceable, and audit-ready
• Embed established data standards, manage metadata and lineage
• Handle complex query and rule versioning to resolve data quality issues
• Collaborate with technical and business teams for high-quality data support
• Influence data governance practices and improve stewardship processes
• Lead efforts for data accuracy and integrity aligned with FDA, EMA, ICH, GxP
• Execute enterprise data governance policies at operational level

Associate Director, Individual Human Data Steward

Project Manager

• Lead end-to-end planning and delivery for a portfolio of Global Medical Operations initiatives
• Establish and run governance rhythms to drive transparency, accountability, and timely decision-making
• Partner with functional leaders to translate strategy into integrated execution plans across evidence generation, scientific communications, grants, and congress/conference deliverables
• Drive cross-functional alignment with internal and external stakeholders, resolving resource conflicts and removing execution barriers
• Own proactive risk, issue, and change management
• Champion continuous improvement by designing, standardizing, and scaling SOPs, templates, and best practices
• Enable high-performing teams by coaching consistent ways of working
• Represent Global Medical Operations on cross-enterprise working groups
• Create and maintain executive-ready reporting
• Coordinate planning and financial forecasting across Scientific Communications, Grants, and Conference Sponsorships
• Provide operational oversight for Global Grants and Donations and Congress/Conference programs
• Own core compliance and audit readiness activities

Project Manager, Global Medical Operations

Manager

• Be the Working Group (WG) Lead for Clinical Operations
• Be accountable for operational delivery of clinical study/studies to time, quality, and budget
• Support decision-making at pace and lead study team to achieve overall study deliverables
• Ensure compliance with ICH/GCP guidelines, all applicable laws and regulations, and GSK SOPs
• Proactively identify, oversee, and mitigate study risks
• Ensure appropriate stakeholder communication, including study status, expectations, risks and issues
• Effectively lead empowered matrix teams
• Implement innovative approaches to study delivery through external facing advances in technology
• Be responsible for operational input into protocol and informed consent form development
• Lead and conduct investigator meetings and ensure continual inspection readiness
• Override the activities of the countries participating in the study

Global Study Manager

• Provide robust analytical insight and business input to drive performance of current and future Specialty Care portfolio in Europe by identifying performance drivers
• Leverage advanced analytics and emerging technologies (e.g. GenAI) to generate insights
• Translate insights into clear calls to action
• Utilize business and marketing experience to identify barriers or enablers to performance
• Contribute to deliver the best product launches thanks to insights
• Partner with Region Europe Head on fact-based recommendations
• Lead monthly EU Operational Excellence and MPR preparation
• Challenge existing thinking and contribute to disruptive commercial tactics
• Develop and lead the regional Specialty insight plan
• Support effective operations of the Regional Specialty Care team and partner with the Regional Specialty Lead and broader team on launch preparations by leading on insight generation and fact-based recommendations to deliver deep market, competitive, and patient pathway insights

Business Insight & Analytics Director, Primary & Specialty Care

• Execute Marketing Analytics within U.S. Pharma Commercial Insights for customer targeting and segmentation, marketing mix modeling, and campaign/program performance analytics
• Proactively identify key opportunities to drive performance by leveraging various Marketing analytics, communicate customer and business insights and data findings, influence decision-making, and drive action to achieve business results
• Collaborate and partner effectively with various stakeholders across the enterprise, including CI, Marketing, Sales, Customer Experience, Finance, and Technology teams; Create succinct story boards to communicate data learnings influencing business decisions
• Continuously identify opportunities to: Bring outside-in thinking: What are other industries and pharma companies doing as a way of best practice understanding and development
• Increase efficiencies through process and analytics automation, as well as partnering with Commercial Data Strategy teams ensuring trusted data availability for standard and ad hoc marketing analytics
• Use analytical tools (SAS, R, Python, or similar) to complete analyses including: Targeting for marketing
• Customer Segmentation
• Segment profiling analytics

Manager, Brand Analytics

• Partner with GRL and Regulatory Matrix Teams and Early/Medicine Development Teams.
• Create and manage integrated regulatory plans.
• Ensure the team is on track to deliver per the Regulatory strategy.
• Collaborate across the R&D matrix for project management and submission oversight.
• Facilitate submission delivery expectations.