Director

• Lead the development and implementation of integrated project schedules across large-scale capital projects.
• Ensure alignment with GSK’s Project Management Framework (PMF), including tools, templates, and best practices.
• Oversee schedule risk analysis using Monte Carlo simulation and other quantitative methods.
• Benchmark schedule performance and establish KPIs for time-related project metrics.
• Provide expert input into project reviews, health checks, and independent project assessments.
• Ownership and management of Schedule management tools such as Primavera P6, MS Project, Oracle Primavera Cloud etc.
• Act as functional lead for planning professionals across the Global Capital Projects (GCP) portfolio.
• Coach and mentor planning and scheduling staff to build internal capability.

Director – Planning & Scheduling

Account Manager

• Build partnerships with large-organized customers
• Achieve and exceed sales targets within the assigned territory
• Identify and engage key influencers
• Plan and organize activities to maximize access and sales opportunities
• Deliver comprehensive clinical brand presentations to healthcare professionals
• Understand the healthcare delivery system within each assigned customer
• Develop in-depth product and competitor knowledge
• Collaborate with peers to share best practices and strategies
• Manage the territory budget

Hepatology Account Manager

• Build partnerships with large-organized customers, incl. IDNs, Academic Centers, and key decision-makers (e.g. Chief Medical Officers, Pharmacy Directors, Infectious Disease Specialists and P&T Committee members)
• Achieve and exceed sales targets within the assigned territory by developing, implementing, and executing an integrated business plan for key accounts to maximize sales
• Identify and engage key influencers, ensuring designated customer interaction expectations are met, with a focus on top target customers
• Plan and organize activities to achieve call metrics, optimizing coverage and frequency to key customers to maximize access and sales opportunities
• Deliver comprehensive clinical brand presentations to physicians and other healthcare professionals, driving appropriate product utilization
• Understand the healthcare delivery system within each assigned customer, including the physician hierarchy, key pharmacy personnel, and clinical nursing staff
• Develop in-depth product and competitor knowledge, staying informed about local and regional market trends
• Analyze local trends to identify long and short-term goals, crafting a robust product launch business plan
• Collaborate with peers in the sales organization to share best practices and strategies
• Provide feedback on marketing strategy, analyze the effectiveness of sales activities and territory performance, and develop territory plans with the Regional Sales Director, brand team, and other support partners to deliver exceptional customer experience
• Manage the territory budget to support sales and marketing activities effectively
• Complete administrative tasks promptly, executing the company brand strategy and tactics within the assigned geographic area
• Participate in training and development programs to enhance skills and knowledge
• Maintain adherence and compliance with all corporate and industry policies and procedures

• Manage a defined territory to build trusted partnerships with oncology care teams.
• Develop and deliver clear territory plans that improve patient access and drive measurable results.
• Collaborate with medical affairs, market access, and commercial operations to solve real challenges for patients and providers.
• Build and maintain trusted relationships with oncologists, nurse navigators, specialty pharmacists, and institutional accounts across your territory.
• Create and execute clear territory business plans that align with regional and national goals.
• Identify high-value prescribers and accounts and focus resources to meet their clinical and operational priorities.
• Partner with cross-functional colleagues to improve patient access and support timely availability of therapies.
• Use customer insights and data to prioritize actions, set measurable goals, and track performance.
• Support launches and local field programs through coordinated, compliant activities.

Oncology Account Manager, Hematology

Medical Director

• Supporting the US Medical Affairs Lead with the development and execution of the US Medical Launch Plan for hepatology.
• Understanding the evolving US healthcare environment (provider/expert) and payer landscape and translating that knowledge into the medical strategy, objectives, and all activities.
• Planning and execution of medical tactics in collaboration with the cross-functional Medical Matrix Team.
• Prioritizing investment in medical activities to deliver the greatest, strategically aligned, impact on patient care measured via GSK’s Medical Impact Framework.
• Leading advice seeking activities and other external engagements to advance scientific and medical understanding of the appropriate development and use of medicines, the management of the disease, and patient care.
• Supporting medical grants, sponsorships, and other collaborations through development of the associated asset strategy.
• Partnering with Medical Communications & Scientific Training and Medical Information stakeholders to ensure communication goals and medical materials created align with the US medicine strategy and business needs.
• In collaboration with field medical, identifying relevant external experts and key on-line influencers and supporting the development of an external engagement plan.
• In partnership with the US Medical Affairs Lead, providing input to shape clinical and health outcomes evidence plans to support anticipated US Market needs.
• Applying sound medical governance for all activities.

Medical Director, Hepatology

Content Writer

• Providing key contributions to clinical document strategy for one or more assets throughout the life cycle of drug development
• Documents in scope include, but are not limited to, clinical study protocols, clinical sections of the IMPD/IND, Investigator’s Brochures, clinical study reports, briefing documents for regulatory authorities, Common Technical Document Summaries and Clinical Overviews, and responses to regulatory authority questions
• Leading matrix teams in planning and production of multiple clinical documents, working with CROs and/or independent contractors as needed
• Planning and successfully delivering large submissions independently, effectively recommending innovative methods and solutions for achieving accelerated timelines
• Assessing and adapting to interdependences of various contributing functions and managing problems affecting timelines as necessary
• Ensuring a global approach for submissions as appropriate, collaborating with Global Regulatory Affairs to ensure business needs and regulatory requirements are met
• Providing guidance and facilitation to submission teams in development of detailed submission plans
• Acting as lead author on submissions
• Effectively organizing content and arguments in complex clinical submission documents, including briefing documents and responses to regulatory questions
• Proposing resourcing solutions for major projects including the number of FTEs required and best use of internal and external resources
• Actively contributing to development of training materials for therapeutic area and providing mentoring and/or training on regulatory requirements, medical writing processes, and submission planning to individuals or teams
• Driving, promoting and implementing key organizational process improvement initiatives
• Proactively generating ideas for simplification and improvement taking advantage of opportunities that arise and challenging the status quo
• Prioritizing and meeting multiple deadlines successfully with attention to detail, demonstrating high performance standards for own work and encouraging similar standards across the matrix
• Promoting leadership behaviors that support GSK values.

Director, Medical Writing Asset Lead

• Build effective, collaborative relationships with external partners and internal stakeholders (eg MW Global Head, MW TA Heads, Finance and Procurement) to align on priorities, resourcing, finance forecasting, vendor onboarding, and contracting.
• Support allocation of work across vendors aligned to capacity and capability and ensure appropriate utilization of vendors to meet project timelines and portfolio demands.
• Define and monitor KPIs and service level agreements (SLAs) for Medical Writing vendors.
• Monitor cost vs. performance to ensure value delivery.
• Lead and conduct regular performance reviews to identify improvement opportunities.
• Drive harmonization of ways of working across vendors.
• Ensure adherence to GSK Third Party Management frameworks, SOPs, and quality standards.
• Ensure risk mitigation plans related to Thirds Party Vendors are implemented and tracked.

Director, Third Party Management – Medical Writing

Supply Chain

• Lead cross-functional supply planning for clinical programs from protocol to patient delivery.
• Create and maintain demand and supply plans, including inventory policy and contingency scenarios.
• Manage clinical packaging, labeling, and distribution activities with internal and external partners.
• Oversee Interactive Response Technology (IRT) specifications, testing and maintenance to support randomization and supply control.
• Proactively identify supply risks and lead mitigation activities to ensure continuity and patient delivery.
• Track program costs, manage budgets and supplier contracts, and report status to stakeholders.

Clinical Supply Chain Manager

• Define and drive the clinical safety and pharmacovigilance strategy for assigned oncology assets in alignment with global business objectives
• Lead safety governance activities, ensuring appropriate escalation, communication, and resolution of emerging safety issues
• Anticipate, identify, and address safety signals, ensuring effective and timely implementation of risk mitigation strategies
• Provide strategic recommendations on benefit-risk profiles to support development and lifecycle management decisions
• Exercise expert scientific judgment in the evaluation and interpretation of complex safety data
• Lead safety data analyses and signal detection activities, ensuring scientifically robust conclusions and documentation
• Guide causality assessments, benefit-risk evaluations, and safety evidence generation across the portfolio
• Oversee proactive identification and assessment of safety signals from clinical trials, post-marketing data, and real-world evidence
• Develop and implement risk management strategies, including labeling updates, risk minimization measures, and stakeholder communication plans
• Lead and influence global, matrixed teams to ensure alignment and execution of safety strategies
• Build strong collaborative relationships across clinical, regulatory, medical, and commercial functions
• Contribute to due diligence activities, including safety assessments for business development opportunities
• Provide strategic oversight and input into regulatory safety documents and responses to Health Authorities

Senior Scientific Director, Oncology

Risk

• Lead global labelling strategy and execution for assigned assets across development and lifecycle stages
• Line manage, coach, and develop a small team of global labelling professionals, building capability and engagement
• Translate clinical and safety data into clear, compliant, and patient-focused labelling content
• Partner with cross-functional teams (regulatory, clinical, safety, medical, and commercial) to align on labelling strategy and deliverables
• Represent the portfolio in labelling governance bodies and ensure alignment with global regulatory requirements and internal standards
• Provide strategic labelling guidance to project teams and senior stakeholders, including implications for development plans and regulatory submissions
• Engage with health authorities, external stakeholders, and professional organizations to support regulatory interactions and contribute to the evolution of labelling practices.

Director – Labelling Strategy and Governance

• Provide expert leadership in clinical safety and pharmacovigilance for oncology assets, including signal evaluation, benefit–risk assessment and proactive risk-management strategies.
• Oversee the review, interpretation and communication of safety data; identify, escalate and manage safety issues through established safety governance forums.
• Develop and implement safety strategies, policies and processes aligned with Global Safety operational and strategic plans.
• Coach and mentor medical and scientific colleagues in SERM in signal evaluation, risk management, and preparation of regulatory safety deliverables.
• Lead within a global, cross-functional matrix, building strong collaborative relationships and influencing internal and external stakeholders on safety topics.
• Lead or oversee SERM safety input into due diligence and other key strategic activities, ensuring safety perspectives shape decision-making.

Senior Medical Director

Platform Engineer

• Serve as a key engineer for the GenAI platform and contribute technical expertise to teams in closely aligned technical areas such as AIML Platform, DevOps, Compute and Cloud.
• Co-design major software components of the GenAI Platform and contribute to development of production code in Python and participate in both design reviews and PR reviews.
• Accountable for key component(s) of GenAI Platform with particular focus on usability, reproducibility and performance at scale
• Integrate with DataOps, and Data Engineering products for best performance and ease of use in ML training at scale
• Participate in scrum teams and contribute technical expertise to teams in closely aligned technical areas.
• Able to design innovative strategies and ways of working to create a better environment for the end users
• Standard bearers for proper ways of working and engineering discipline, including CI/CD best practices and proactively contribute to improvements within your engineering area.

Senior Gen AI Platform Engineer

• Build partnerships with large-organized customers, including IDNs, Academic Centers, and key decision-makers
• Achieve and exceed sales targets within the assigned territory by developing, implementing, and executing an integrated business plan for key accounts
• Identify and engage key influencers
• Plan and organize activities to achieve call metrics
• Deliver comprehensive clinical brand presentations to physicians and other healthcare professionals
• Understand the healthcare delivery system within each assigned customer
• Develop in-depth product and competitor knowledge
• Analyze local trends to identify long and short-term goals
• Collaborate with peers in the sales organization
• Provide feedback on marketing strategy
• Manage the territory budget to support sales and marketing activities

• Provides advanced scientific expertise in the safety evaluation and risk management of key GSK oncology assets in clinical development.
• Leads the identification, assessment, and communication of safety risks to ensure robust benefit-risk profiles and protection of patients globally.
• Drives the evaluation and interpretation of safety data, including signal detection and assessment.
• Develops strategic approaches for safety issue evaluation within clinical development programmes.
• Contributes to safety components of global regulatory submissions (e.g., INDs, DSURs, IBs).
• Ensures high-quality, timely delivery while managing multiple priorities.
• Represents Safety Evaluation & Risk Management (SERM) on Clinical Matrix and Project Teams.
• Leads cross-functional efforts to address urgent and complex product safety issues.
• Partners closely with Safety Physicians and stakeholders to prepare for and contribute to Safety Review Team (SRT) meetings.
• Escalates emerging safety issues to senior leadership and governance bodies as appropriate.
• Communicates complex scientific information clearly to a range of audiences.

Director – Planning & Scheduling

Hepatology Account Manager

Hepatology Account Manager

Oncology Account Manager, Hematology

Medical Director, Hepatology

Director, Medical Writing Asset Lead

Director, Third Party Management – Medical Writing

Clinical Supply Chain Manager

Medical Director, Hepatology

Senior Scientific Director, Oncology

Director – Labelling Strategy and Governance

Senior Medical Director

Senior Gen AI Platform Engineer

Hepatology Account Manager

Scientific Director, SERM