Director

• Lead key activities to progress your career in quantitative clinical pharmacology
• Contribute to the design of clinical development program and support life cycle management of an asset
• Provide application of Clinical Pharmacokinetic (PK), Pharmacodynamic (PD), and Modeling & Simulation (MS) principles towards efficient drug development
• Predict human dose range, characterize exposure-response relationship and justify dose recommendations
• Develop mathematical models to understand disease and drug pharmacodynamics
• Write sections of drug development documents and clinical trial protocols

Director, Quantitative Clinical Pharmacologist

Manager

• Supports access to GSK Oncology products for appropriate patients
• Responsible for educating providers on payer coverage, coding and payment policies related to GSK Oncology products
• Helping providers understand GSK Patient Support Programs intended to help appropriate patients access GSK Oncology medicines
• Routinely interface internally with Payer Account Managers, Specialty Pharmacy Account Directors and Oncology Sales professional teams
• Analyze access/reimbursement issues and opportunities
• Provide offices product access/reimbursement expertise
• Provide access/reimbursement education to field teams
• Coordinate on access/reimbursement issues with third parties including hubs
• Support patient access to the products by providing subject matter expertise on reimbursement issues that may be barriers to product access

Manager, Access & Reimbursement – Oncology

• Development and execution of precision diagnostics strategy for oncology programs, spanning multiple assets and therapeutic areas.
• Define diagnostic requirements for trials and, in partnership with clinical teams, implement biomarker selection, assay validation, and biological sample collection/handling strategy.
• Oversee project plans, budgets, and timelines to ensure on-time, high-quality delivery of diagnostic milestones via cross-functional collaboration with project management, biomarkers, clinical & biomarker operations, external engagement, procurement, etc.
• Work with regulatory and quality teams to ensure diagnostic development meets regulatory expectations and requirements and in diagnostic regulatory submissions.
• Engage external partners, including diagnostic companies, clinical labs and technology vendors, to accelerate assay development and access to patient samples.
• Provide frequent project status updates and reports related to diagnostic deliverables in collaboration with project management, finance and business operations.
• Share learnings and best practices for diagnostic development and execution and participate in initiatives for key organizational process improvements.

Director – Precision Diagnostics, Oncology

• Responsible for the development and effective implementation of biomarker and translational medicine strategies to support the clinical development of late-stage oncology assets.
• Collaborate with the Clinical Biomarker Executive Director to drive the design, alignment, and execution of clinical biomarker and translational medicine strategies.
• Validate and implement biomarker strategies for clinical-phase programs to support patient stratification.
• Participate in tumor-specific Biomarker Matrix teams, executing clinical biomarker strategies for late-stage oncology programs.
• Represent Translational Medicine at Clinical Development Matrix Teams to establish biomarker-driven decision-making criteria.
• Oversee and/or develop sample testing plans and deliver high-quality biomarker data packages.

Director, Oncology Clinical Biomarkers

• Accountable for the epidemiology program for at least one asset or disease area
• Proposing and negotiating program content and budget with matrix leaders
• Developing a Global Epidemiology Plan
• Liaising with relevant stakeholders
• Providing expert epidemiological insights to asset matrix teams
• Leading and overseeing complex epidemiological studies
• Identifying and building new opportunities, methods, and external partnerships
• Leading departmental initiatives driving innovative solutions
• Managing and mentoring junior staff,
• Representing GSK in scientific interactions
• Planning and coordinating scientific dissemination of epidemiology data
• Partnering with external groups conducting epidemiological studies globally

Director, Epidemiology, Hepatology

Supply Chain

• Partner with SCT work stream SMEs, GPOs, the Systems Integrator and Business Integrators to support identification of training needs, knowledge assets and other process documentation requirements
• Work with GSK People Capability colleagues to support analysis of existing process documentation and training courses
• Collaborate with SMEs, GPOs, System and Business integrator to develop documentation and training materials
• Support development of training programmes for demand and supply planning personas
• Publish and manage knowledge resources on the GSK knowledge platforms
• Deliver process, OMP solution trainings as a part of the deployment of OMP
• Provide on job support and coaching for planning personas post go live
• Support the Program delivery governance by generating status reports related to training
• Continuously improve training approach and assets.

Supply Chain Transformation Training Subject Matter Expert, Supply

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.
• 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, act as an individual contributor or may have direct line management responsibilities as per business needs.

Director, CMC Regulatory Affairs

Project Manager

• Take ownership for multiple complex CMC regulatory submissions, including planning, coordination and execution, to support applications for marketing authorizations, lifecycle activities and maintenance of registered products across Vaccines portfolio, in accordance with the applicable regulatory and scientific standards.
• Manage multiple project assignments simultaneously, including CMC variations and handling Health Authority Questions (HAQs) for Finished Products, Intermediates, and Active Pharmaceutical Ingredients for Vaccines products (i.e. largely involving updates to the CTD Module 3, Quality section of the dossiers).
• Identify risks associated with submission data and information package; and support the development of mitigation strategies.
• Collaborate closely with cross-functional teams, such as Global Regulatory Lead’s team, Global Supply Chain (GSC), Quality Assurance (QA), Local Operating Companies (LOCs), and third Parties to build regulatory CMC submissions and maintain strong relationships, including with senior stakeholders.
• Identify improvement opportunities for CMC Regulatory processes, policies, instructions and systems, developing and implementing simplified working practices and procedures to enhance efficiency and quality.
• Serve as Subject Matter Expert (SME) for CMC Regulatory Affairs, mentoring and guiding team members, while sharing best practices to build capability and knowledge within the CMC Regulatory teams and other impacted functions.

Regulatory Project Manager

• Être un leader stratégique au cœur de la performance et de l’évolution du site de Ste‑Foy
• Piloter la fonction MSAT et agir comme Responsable Produit pour les produits de la franchise Grippe
• Orienter la stratégie des procédés, la validation, les standards technologiques et les initiatives d’amélioration continue
• Assurer la robustesse des procédés, la conformité réglementaire et la performance durable des produits tout au long de leur cycle de vie
• Diriger une équipe multidisciplinaire
• Optimiser la performance opérationnelle, sécuriser la fiabilité des livraisons et développer les capacités techniques du site

Directeur de site, Sciences et technologies de la fabrication

• 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

Sterility Assurance Excellence Lead – Senior Director

Executive Assistant

• Provide high-quality executive support to senior leaders in a fast-moving, global environment
• Manage complex calendars, travel, and meetings while building strong relationships across functions
• Coordinate international travel, visas, and detailed itineraries, anticipating issues and resolving conflicts proactively
• Prepare high-quality meeting materials, leadership briefs, and presentations for senior-level forums
• Act as a central coordination point for leadership meetings, governance forums, and cross-functional interactions
• Build trusted relationships with senior stakeholders and executive assistants across the organisation
• Lead process improvements and operational support activities, including expenses, invoices, and purchase requests

• Management of marketing authorizations (MAs) and coordination of associated activities for assigned markets including the primary interface with Content Delivery and 3rd Party Service Provider to support regulatory submissions to local regulatory agencies
• Effective planning and tracking of regulatory activities for defined markets
• Ensures that GSK Labeling (PI/PIL) is compliant with MA and with regulatory requirements and available in local language as applicable
• Co-ordinates the completion of local language translations by 3rd Party CRO (as applicable)
• Ensures product information is compliant with MA and product pack changes are implemented in compliance with regulations and aligned to supply chain planning
• Co-ordinates all regulatory submissions and commitments, ensuring these are in alignment with regulatory requirements and agreed strategy and timelines
• Co-ordinates with Content Delivery the management of product registration documents and agency correspondence in regulatory databases and repositories
• Builds and maintains effective relationships with, and provide considered regulatory advice, leadership, and expertise to cross functional stakeholders
• Effective communication, collaboration, planning and oversight of Regulatory Third-Party service providers to achieve Regulatory objectives and meet compliance standards
• Participation and compliance in internal and external projects and activities
• Lead Resource management, objective setting, performance and development of staff, talent reviews and succession planning, through a coordinated, well managed, strategically aligned program
• Monitor and keep abreast of changes in the regulatory environments. Provide intelligence to relevant stakeholders and central teams on potential impact changes in the regulatory environment in the region

Regulatory Affairs Manager, CIS/Asia Cluster

Medical Director

• Provide clinical and scientific insights to potential new, established and emerging assets in clinical development with a strong focus on liver diseases
• Work within project teams to plan, execute, and deliver clinical development activities up to and including registrational studies
• Ensure clinical excellence, regulatory compliance, and operational efficiency
• Design and execute clinical development plans across advanced stages of development
• Input to, and may lead, regulatory interactions and documents including briefing documents, presentations
• Provide medical monitoring and oversight of the safety of study participants on behalf of the Sponsor during the study
• Act as clinical lead for a clinical study, taking a key role on the Study Leadership Team
• Evaluate specific business development activities, including due diligence and contributes to the implementation and embedding of strategic/organizational initiatives

Medical Director, Clinical Development, Hepatology

Sales

• Lead, manage, and develop the skill sets and overall performance of the account managers in the region.
• Recruit, hire, train, develop, and coach account managers to ensure a high-performing team.
• Drive awareness, understanding, utilization and sales of a launch product through leading, managing and developing the skill sets of the account managers in the region.
• Develop and implement business plans to contribute to overall project success and achieve organizational objectives.
• Provide effective leadership to the sales team to compliantly meet and exceed sales targets.
• Execute the approved marketing plan with the regional team to maximize market penetration.
• Identify and monitor local market conditions to build strong customer relationships and adapt strategies accordingly.
• Ensure compliance with all field activities and company guidelines.
• Ensure timely and effective delivery of marketing and sales tactics within the region.
• Collaborate on goal setting and performance measures at all levels to ensure achievement.
• Utilize reports and tools from Analysis & Reporting to monitor goal attainment as per client agreements.
• Establish clear performance expectations and oversee direct reports' activities to ensure policy adherence, while providing continuous feedback to foster a supportive, team-oriented environment.
• Conduct regular field ride-alongs with account managers to provide hands-on coaching.
• Manage the performance management process for all team members, ensuring fair and timely resolution of disciplinary issues.
• Foster a rewarding environment that encourages accomplishment and the advancement and retention of productive employees.

Regional Sales Director

Account Manager

• Manage a defined territory in San Antonio to build trusted partnerships with oncology care teams.
• Create and deliver clear territory plans that improve patient access and drive measurable results.
• Work closely with colleagues in medical affairs, market access, and commercial operations.
• 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 needs and priorities.
• Partner with cross-functional colleagues to improve patient access and ensure timely availability of therapies.
• Use customer insights and data to prioritize actions, set measurable goals, and track performance.
• Support local launches and field programs through coordinated, compliant activities.