Future Tech Jobs
Future Tech Jobs
GSK Oncology is committed to discovering and developing new therapies with the potential to change the lives of patients with cancer. The Oncology Clinical Development Statistics group is seeking exceptionally talented Statisticians to provide end-to-end statistical leadership across oncology evidence...
This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive successful collaborations.
This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regional and global regulatory leads, partnering with directors on innovative regulatory strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.
In this laboratory-based role, you will design, express, purify, and characterize recombinant proteins to support biologics discovery and development. Your work will directly impact the evaluation of novel therapeutic modalities and inform clinical decisions, using modern computational tools and rigorous experimental methods.
Provides strategic legal counsel for GSK's Global Supply Chain, focusing on transactions, disputes with contract manufacturers, and external manufacturing agreements. Acts as a key business partner to senior stakeholders, negotiating complex contracts, supporting business development deals, and managing legal risks across pharma and vaccines operations. Works collaboratively within a global legal network to deliver aligned, proactive legal solutions in a highly regulated environment.
This role leads the global development of a respiratory medicine from clinical proof of concept through to regulatory approval, serving as the primary accountable leader across a matrixed cross-functional team. The VP will define strategic direction, oversee clinical and regulatory planning, manage budgets, and ensure alignment with GSK’s broader R&D and commercial objectives. The position involves high-level stakeholder engagement, lifecycle planning, and external representation to regulators and advisory bodies.
Lead the global development of a respiratory medicine from clinical proof of concept through to first-market approval, serving as the single point of accountability. You will build and lead a cross-functional matrix team, define strategic direction, and ensure alignment with GSK’s R&D and commercial strategies. The role involves shaping lifecycle plans, making evidence-based go/no-go decisions, and engaging with regulators and senior leadership to deliver patient-focused medical solutions.
Leads global development of a respiratory medicine from clinical proof of concept to approval, aligning cross-functional teams across R&D, manufacturing, and commercial functions. Defines strategic vision, manages development plans, regulatory submissions, and lifecycle strategy while ensuring patient-focused innovation and compliance. Acts as primary point of accountability and spokesperson to senior leadership and external stakeholders.
This role leads the global development of a respiratory medicine from proof of concept through to approval, serving as the primary accountable leader across a cross-functional matrix team. The VP will define strategic direction, oversee clinical and regulatory execution, and align development with GSK’s broader R&D and commercial strategy, while engaging with senior leadership and external stakeholders to advance patient-focused innovation.
Leads global development of a respiratory medicine from clinical proof of concept through approval, serving as the primary accountable leader across a cross-functional matrix team. Defines strategic vision, drives evidence generation, lifecycle planning, and regulatory strategy while coordinating input from R&D, manufacturing, commercial, and regulatory stakeholders to deliver patient-focused therapies.
Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.
Lead CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Work cross-functionally to ensure compliance, support inspections, and maintain product supply. Influence regulatory decisions and mentor teams within a complex, matrixed environment.
Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works across cross-functional teams to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions in a complex, global environment.
Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, coordinating technical submissions and ensuring compliance with global regulations. Works cross-functionally to address complex CMC issues, support inspections, and influence regulatory decisions. Focuses on maintaining product supply and optimizing regulatory processes across international markets.
Leads CMC regulatory strategy for biopharmaceutical development and lifecycle management, ensuring compliance with global regulations and supporting submissions, inspections, and supply continuity. Works cross-functionally to shape regulatory approaches and mentor teams, with a focus on innovation and risk mitigation in complex regulatory environments.
