Leads clinical operations strategy across the full asset lifecycle, ensuring high-quality, on-time delivery of clinical studies. Works cross-functionally to shape clinical development plans, manage vendor and resourcing strategies, and maintain inspection readiness. Focuses on patient-centric, efficient study execution within a global, matrixed environment.
Leads clinical operations strategy and execution across the full lifecycle of a drug development asset, ensuring high-quality, compliant, and efficient delivery of global clinical trials. Works cross-functionally to shape development plans, manage risk, and align operational delivery with scientific and regulatory goals. Provides strategic leadership to study teams and represents clinical operations at senior governance levels.
This role involves designing and executing bioanalytical and immunogenicity strategies to support mRNA-based clinical development programmes. The scientist will lead assay development—including ADA, nAb, PK, and PD assays—using platforms like ELISA, MSD, and cell culture, while ensuring regulatory compliance and contributing to Moderna's expanding capabilities in Harwell. The position emphasizes collaboration across multidisciplinary teams and integration of digital and AI-enabled tools to enhance data interpretation and decision-making.
This role involves shaping and driving CMC regulatory strategies for UK-manufactured and UK-licensed mRNA products, from development through commercialisation and post-approval lifecycle management. You will work with cross-functional teams to ensure regulatory compliance and navigate complex MHRA requirements, contributing to global regulatory strategies and leading regulatory submissions.
This role involves leading the creation and management of investigator site budgets and contracts for clinical trials, using Grants Manager and FMV benchmarking tools. The candidate will oversee CRO activities, ensure budget consistency across trials, and support timely site activation by managing negotiations and identifying risks. Collaboration with legal, clinical operations, and external partners is central to ensuring compliance and efficiency in contract execution.
The Principal Programmer Analyst role involves leading statistical programming activities for clinical studies, ensuring high-quality and timely outputs. You will collaborate with cross-functional teams, mentor junior programmers, and support regulatory interactions, working in an agile, squad-based environment.
This role involves leading programming activities for clinical studies, ensuring high-quality and timely outputs. Responsibilities include mentoring junior programmers, fostering quality assurance, and collaborating with cross-functional teams to bridge scientific requirements with technical solutions.
The Principal Programmer Analyst role involves leading programming activities for clinical studies, ensuring high-quality and timely outputs. Responsibilities include mentoring junior programmers, supporting regulatory interactions, and implementing innovative solutions to improve efficiency and compliance.
Lead the strategy and development of AI-enabled digital products for structured authoring of regulatory and clinical evidence content across GSK’s R&D function. Drive innovation in modular content management, automation, and AI-assisted workflows while ensuring compliance with GxP and data integrity standards. Collaborate with cross-functional scientific and technical teams to scale enterprise-grade solutions.
This role involves leading the clinical development of oncology drugs, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the asset in external engagements. The role emphasizes data-driven decision-making and leveraging advanced analytics to enhance development speed and precision.
This role involves leading the clinical development of oncology GU (genitourinary) treatments at GSK, defining the clinical strategy, and serving as the clinical authority for the asset. Responsibilities include strategic planning, governance, and external engagement with health authorities and advisory boards.
This role involves leading the strategic execution of external data partnerships to enhance R&D and CPO activities. Responsibilities include defining and delivering RWD partnerships, maintaining data quality, and fostering relationships with academic institutions, health technology companies, and data holders to support regulatory approval and evidence generation.
This role involves leading the clinical development of oncology drugs, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the company in health authority interactions. The role emphasizes data-driven decision-making and leveraging advanced analytics to enhance clinical development.
This role involves leading the clinical development of oncology drugs, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the company in health authority interactions. The position requires strong scientific and leadership skills, with a focus on leveraging data and technology to drive clinical development.
This role involves leading the clinical development of oncology treatments, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the asset in external engagements. The role emphasizes data-driven decision-making and leveraging advanced analytics.
