Latest Technology Jobs

Senior Director, Portfolio Integration Lead - Hematology

Leads cross-programme scientific strategy and integration across GSK’s hematology oncology portfolio, ensuring alignment in clinical development, biomarker strategies, and innovative trial design. Acts as a senior scientific partner to Clinical Development Leads and drives data-driven decision-making using emerging technologies like AI. Operates at the portfolio level to shape disease-area strategy and support regulatory and governance engagement.

GSK US$242,250 – US$403,750 pa

Hybrid Permanent

Senior Director, Portfolio Integration Lead - Hematology

Lead scientific and strategic integration across GSK's hematology oncology portfolio, ensuring alignment of clinical development programmes, biomarker strategies, and innovative trial designs. Drive cross-asset coordination and decision-making at the disease level, leveraging deep oncology expertise and emerging technologies like AI. Engage with internal stakeholders and external experts to shape portfolio direction and regulatory strategy.

GSK US$242,250 – US$403,750 pa

Hybrid Permanent

Senior Clinical Research Associate II

This role involves managing and monitoring clinical trial sites to ensure compliance with regulatory standards, patient safety, and study quality. The Senior Clinical Research Associate will serve as the primary point of contact for investigator sites, conduct onsite and remote monitoring, resolve protocol issues, and support enrollment and database release activities. The position requires extensive knowledge of GCP, ICH guidelines, and experience in clinical trial operations, particularly in oncology or related therapeutic areas.

Pfizer United Kingdom

Remote Permanent

Innovation, Data & Analytics Team, Senior Manager, Data Scientist

A Senior Manager, Data Scientist in Pfizer's Innovation, Data & Analytics (IDA) Team leads the design and implementation of advanced analytical and AI-driven solutions to support data-informed decision-making across Medical Affairs. The role involves developing machine learning and natural language processing models, defining evaluation frameworks, and translating complex medical and business questions into robust analytical approaches. Collaboration with data engineering, AI/ML teams, and governance stakeholders is central, with an emphasis on responsible AI, scalability, and production-ready workflows using real-world healthcare data.

Pfizer

Senior Director, Portfolio Integration Lead - Hematology

This role leads cross-programme scientific strategy and integration across GSK’s hematology oncology portfolio, ensuring alignment in disease biology, biomarker development, and clinical trial innovation. The individual will drive portfolio-level decision-making, shape clinical development approaches using emerging technologies like AI, and engage with external experts and regulatory bodies. It is a senior individual contributor position focused on strategic coherence across multiple assets rather than direct management of a single programme.

GSK US$242,250 – US$403,750 pa

Hybrid Permanent

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and execute model-informed drug development strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize dose selection, trial design, and regulatory submissions. Work across multidisciplinary teams to drive quantitative decision-making in clinical pharmacology and contribute to the development of innovative cancer therapies.

GSK United States £188,100 – £313,500 pa

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and execute model-informed drug development strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize clinical trial design, dose selection, and regulatory submissions. Drive innovation in quantitative clinical pharmacology across the R&D pipeline, from early development through lifecycle management, within a multidisciplinary translational medicine team.

GSK £119,250 – £198,750 pa

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and deliver model-informed drug development (MIDD) strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize clinical trial design, dose selection, and regulatory submissions. Work across multidisciplinary teams to advance GSK’s oncology pipeline using quantitative approaches including exposure-response modeling, disease progression models, and simulation-based trial design. Drive innovation through external collaborations, publications, and adoption of cutting-edge methodologies in clinical pharmacology.

GSK

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and execute model-based drug development strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize dose selection, trial design, and regulatory submissions. Drive innovation in clinical pharmacology through cross-functional collaboration and external engagement. Operate in a science-driven environment focused on accelerating the development of novel cancer therapies.

GSK US$188,100 – US$313,500 pa

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead clinical pharmacology and modelling & simulation efforts for oncology drug development, applying AI/ML and quantitative methods to optimise dosing, trial design, and regulatory strategy. Drive innovation in model-informed drug development across small molecules, biologics, and antibody-drug conjugates. Collaborate with cross-functional teams to accelerate therapies to patients using advanced pharmacometric and machine learning techniques.

GSK £188,100 – £313,500 pa

Engineering Technician (numerous vacancies)

This role involves providing engineering support across manufacturing operations at GSK’s Ware site, performing electrical and mechanical maintenance, calibration, fault diagnosis, and continuous improvement activities on production and utilities equipment. Technicians work in regulated GMP environments across respiratory, oral solid dose, or facilities teams, ensuring compliance with safety and quality standards. The role includes shift work and collaboration with cross-functional teams to maintain high-throughput pharmaceutical manufacturing.

GSK East Hertfordshire, United Kingdom

On-site Permanent Shift-work

Principal Medical Writer

This role involves authoring and delivering high-quality clinical regulatory documents such as protocols, Clinical Study Reports, and submission dossiers for global regulatory agencies. The Principal Medical Writer will lead complex writing projects, collaborate with cross-functional teams, and translate clinical and statistical data into clear, compliant narratives. The position emphasizes leadership in document strategy, regulatory interpretation, and the use of automation tools within a hybrid work environment.

GSK Stevenage, United Kingdom CA$118,000 – CA$168,000 pa

Hybrid Permanent

Supported Studies Asset Study Delivery Lead - 14 month secondment

Leads end-to-end delivery of clinical study portfolios for a specific asset, coordinating proposal reviews for investigator-initiated and collaborative studies. Manages milestone tracking, budget forecasting, supply coordination, and stakeholder communication across cross-functional teams. Acts as primary operational contact and provides oversight in compliance with GCP and regulatory standards, while supporting team development and process improvements.

GSK United Kingdom

Contract

Principal Medical Writer

Author and deliver high-quality clinical regulatory documents such as protocols, Clinical Study Reports (CSRs), and Investigator’s Brochures. Lead the development of clinical dossier submissions, interpret complex clinical and statistical data, and collaborate with cross-functional teams to ensure regulatory compliance and timely delivery. Work within a hybrid model, balancing remote and in-office settings, while supporting global submissions across key therapeutic areas.

GSK CA$118,000 – CA$168,000 pa

Principal Medical Writer

Author and lead the development of high-quality clinical regulatory documents such as protocols, Clinical Study Reports, and CTD submissions. Interpret complex clinical and statistical data to produce accurate, compliant narratives. Collaborate with cross-functional teams and manage complex writing projects across therapeutic areas and global submissions.

GSK CA$118,000 – CA$168,000 pa

Hybrid Permanent