Future Tech Jobs
Future Tech Jobs
The Audit Senior Lead role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the EMEA region. Key responsibilities include evaluating compliance, managing stakeholder engagement, and producing clear audit reports to mitigate risks and ensure regulatory adherence.
This role involves performing and managing GMP and compliance audits of biopharmaceutical, vaccine, and pharmaceutical facilities across the GSK Global Supply Chain. You will evaluate compliance with regulatory requirements and provide sterile manufacturing expertise, engaging with senior stakeholders and producing clear audit reports.
This role leads clinical operations for high-impact, complex global trials in hepatology, renal, and cardiovascular disease, with a focus on late-phase outcomes studies and rare diseases. The position shapes operational strategy, drives innovation in trial design, and ensures delivery across a diverse asset portfolio. It involves leading vendor partnerships, managing regulatory and quality compliance, and developing clinical teams within a patient-ambitious, data-driven environment.
This role leads clinical strategy and scientific vision for oncology assets focused on lung and head/neck cancers, shaping end-to-end development from discovery to approval. The Executive Medical Director acts as the principal clinical authority, integrating advanced analytics and AI-driven insights to accelerate decision-making, while representing Clinical Development in governance, regulatory interactions, and external collaborations. They will mentor talent and drive innovation across a dynamic, matrixed R&D environment.
This role leads clinical operations for complex, multi-indication assets in hepatology, renal, and cardiovascular disease, with strategic oversight of global Phase III trials, rare disease programmes, and co-development partnerships. The position involves shaping operational strategy, managing high-level vendor relationships, and driving innovation in trial design including decentralised and hybrid models. It requires leadership in risk management, data-driven decision-making, and team development within a global regulatory and compliance framework.
This role leads clinical operations for high-complexity assets in hepatology, renal, and cardiovascular disease, with a focus on global Phase III outcomes trials, rare disease programmes, and co-development partnerships. The position drives end-to-end operational strategy, including country and site selection, patient recruitment, risk management, and vendor oversight, while ensuring alignment with clinical development and evidence generation plans. It also involves direct leadership of clinical teams, fostering innovation in trial design, and maintaining inspection readiness across the portfolio.
This role leads clinical operations for high-impact, complex global trials in hepatology, renal, and cardiovascular disease, with a focus on late-phase outcomes studies and rare diseases. The position involves shaping operational strategy, managing CRO partnerships, and driving innovation in trial design while ensuring quality and compliance. Leadership includes direct management of clinical teams and strategic input into asset development across the R&D pipeline.
This role leads clinical operations for complex, high-impact assets in hepatology, renal, and cardiovascular disease, with responsibility for global Phase III trials, rare disease programmes, and co-development partnerships. The position involves setting operational strategy, managing CROs and vendors, driving data-led decision-making, and ensuring trial delivery to time, cost, and quality. It also includes direct leadership of clinical operations teams and integration of innovative trial methodologies.
This role leads clinical operations for high-complexity assets in hepatology, renal, and cardiovascular disease, with a focus on global Phase III outcomes trials, rare disease programmes, and co-development partnerships. The position drives operational strategy, risk management, and innovation in trial design, while managing senior vendor relationships and developing clinical teams. It emphasizes data-led decision-making, enterprise-wide impact, and compliance across a global development portfolio.
This role leads clinical strategy for oncology assets focused on lung and head/neck cancers, shaping end-to-end development plans and scientific narratives across the asset lifecycle. The Executive Medical Director acts as the principal clinical authority, aligning cross-functional teams on strategic decision-making, benefit-risk frameworks, and regulatory positioning. They leverage advanced analytics and AI-driven insights to accelerate data-informed decisions while representing Clinical Development in governance, external engagements, and talent development.
This role leads the clinical strategy for oncology assets focused on lung and head/neck cancers, defining the scientific narrative, benefit-risk framework, and development roadmap across the asset lifecycle. The Executive Medical Director acts as the clinical authority, shaping strategic decisions, governance, and external engagement while leveraging AI and advanced analytics to accelerate development. They lead talent development and ensure alignment across clinical, regulatory, and commercial functions to deliver impactful cancer therapies.
This role leads the clinical strategy and scientific narrative for oncology assets focused on lung and head/neck cancers, shaping end-to-end development from discovery to approval. The Executive Medical Director acts as the strategic leader within cross-functional teams, driving integrated decision-making, regulatory engagement, and evidence generation using advanced analytics and AI. They are responsible for mentoring talent, influencing enterprise-level governance, and ensuring clinical development aligns with patient needs and commercial readiness.
This role leads clinical strategy for oncology assets focused on lung and head/neck cancers, defining the scientific narrative and benefit-risk framework across the development lifecycle. The Executive Medical Director serves as the primary clinical authority, shaping strategic decisions, guiding regulatory engagement, and integrating insights from data and technology to accelerate impactful therapies. They will mentor clinical talent and drive innovation in development models within a global biopharma environment.
This role leads clinical strategy and scientific vision for oncology assets focused on lung and head/neck cancers, shaping end-to-end development from discovery to approval. The Executive Medical Director drives integrated decision-making across regulatory, commercial, and clinical domains, leveraging advanced analytics and AI to accelerate impactful therapies. They serve as a key governance leader and external representative, ensuring strategic alignment across functions and stakeholders.
This role focuses on driving AI innovation in clinical development by identifying operational bottlenecks, designing and running AI pilots, and translating findings into scalable solutions. The person will work across clinical operations, technology teams, and vendors to validate AI tools, generate evidence of value, and guide investment decisions. Emphasis is placed on hands-on testing, change management, and enterprise-wide adoption of AI-native capabilities.
