Future Tech Jobs
Future Tech Jobs
Latest UK roles, updated daily.
The Head, Oncology Clinical Development- ADCs, will report to the SVP, Head of Oncology Clinical Development. The role holder will be accountable for the design and implementation of the clinical development strategy across a particular asset across multiple tumor types...
This role involves providing strategic HR leadership to support ViiV Healthcare’s mission-driven goals, partnering with senior leaders to shape talent, culture, and organisational development across global functions. The HR Business Leader will drive change management, leadership development, and talent strategy alignment with business objectives in a fast-paced, global HIV-focused environment.
This role leads scientific and strategic integration across GSK’s hematology oncology portfolio, ensuring alignment and innovation in clinical development. The Senior Director acts as a cross-functional thought partner to Clinical Development Leads, shaping disease-level strategies, biomarker approaches, and trial innovation. They drive portfolio coherence, data-driven decision-making, and engagement with external experts to advance impactful cancer therapies.
This role leads cross-programme scientific strategy and integration across GSK’s oncology portfolio, with a focus on hematology. The Senior Director ensures alignment in clinical development, biomarker strategy, and trial innovation across multiple assets, acting as a scientific partner to Clinical Development Leads and shaping portfolio-level decision-making. The position emphasizes data-driven innovation, external engagement, and strategic coherence in a matrixed R&D environment.
Leads scientific and strategic integration across GSK's hematology oncology portfolio, ensuring alignment, innovation, and clinical excellence across multiple development programmes. Acts as a senior scientific partner to clinical teams, shaping biomarker strategies, trial designs, and portfolio-level decision-making in a matrix environment.
Leads cross-program scientific strategy and integration for GSK's hematology oncology portfolio, ensuring alignment across clinical development teams and driving innovation in trial design and data use. Acts as a senior scientific advisor to clinical leads, shaping development pathways through disease-level insights and external engagement. Focuses on advancing precision medicine, biomarker strategies, and novel combinations across multiple assets.
This role involves providing scientific leadership across GSK's hematology oncology portfolio, ensuring strategic alignment and integration across multiple clinical development programs. The Senior Director will drive innovation in trial design, biomarker strategies, and data-driven decision-making while serving as a key advisor to clinical teams and external stakeholders. The position requires deep expertise in oncology drug development and the ability to shape cross-asset portfolio strategy.
Leads cross-programme scientific strategy and integration for GSK's hematology oncology portfolio, ensuring alignment across clinical development, biomarker strategies, and innovation initiatives. Acts as a senior scientific partner to clinical teams, drives portfolio-level decision-making, and shapes engagement with external experts and regulatory bodies. Focuses on advancing novel therapies through data-driven insights, clinical trial innovation, and precision medicine approaches.
This role involves providing end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through manufacturing and commercialization. The Molecule Steward ensures product quality, regulatory compliance, and process robustness by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives. It requires deep scientific expertise, strong leadership in matrixed environments, and coordination across R&D, manufacturing, and regulatory functions.
This role involves end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through manufacturing and commercialization. The Molecule Steward ensures product quality, robustness, and compliance by leading technical strategy, process optimization, and cross-functional collaboration across R&D, manufacturing, and regulatory teams. They play a key role in technology transfer, continuous process verification, and maintaining control strategies in a highly regulated environment.
This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development through manufacturing and commercial supply. The Molecule Steward ensures product quality, process robustness, and regulatory compliance by leading technical strategy, coordinating cross-functional teams, and driving continuous improvement across global supply chain sites. The position requires deep scientific expertise, strong leadership in matrixed environments, and active involvement in regulatory submissions and lifecycle management.
This role involves providing end-to-end technical leadership for a pharmaceutical product throughout its lifecycle, from development to commercial manufacturing. The Molecule Steward ensures product quality, robustness, and manufacturability by leading technical strategy, process optimization, and regulatory compliance across global supply chain teams. The position requires deep scientific expertise, cross-functional collaboration, and leadership in resolving complex technical challenges in a regulated environment.
This role involves leading high-impact transformation initiatives within Drug Development and Supply (DDS) at GSK, focusing on process optimization, organizational change, and performance enablement. The Director will act as a cross-functional integrator, driving strategic programs and ensuring adoption of new ways of working across a complex, matrixed biopharma environment.
This role involves leading clinical development for oncology assets, specifically in genitourinary (GU) cancers, within a global matrix environment. The Senior Medical Director will design and execute Phase 1–3 clinical trials, ensure scientific integrity of study data, and collaborate with internal and external experts to advance GSK’s oncology pipeline. Key responsibilities include real-time medical monitoring, regulatory engagement, and shaping clinical strategy to support drug development and lifecycle management.
This role leads clinical development for genitourinary (GU) oncology programs within GSK’s global oncology portfolio, focusing on designing and executing Phase 1–3 trials. The Senior Medical Director will provide medical oversight, interpret clinical data, and collaborate with internal and external experts to advance innovative cancer therapies from development through regulatory approval and market launch.
