Latest Technology Jobs

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities to advance GSK’s oncology portfolio. Key responsibilities include developing and executing phase 1-3 clinical trials, collaborating with cross-functional teams, and engaging with key external experts to ensure the successful development and regulatory approval of innovative oncology treatments.

GSK United States

Hybrid Permanent

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead the clinical research and development of GSK’s oncology portfolio, collaborating with various stakeholders to design and execute phase 1-3 clinical trials. Key responsibilities include medical oversight, protocol development, data interpretation, and engagement with key external experts to ensure the successful regulatory filing and market launch of innovative oncology treatments.

GSK

Hybrid Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing Medical Insights processes, collaborating with various stakeholders to generate actionable insights, and embedding these insights into medical decision-making. The role focuses on advanced analytics, AI, and emerging technologies to inform Pfizer's medical strategies and improve the value of medical insights.

Pfizer

On-site Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing Medical Insights processes, collaborating with various stakeholders to generate actionable insights, and embedding these insights into medical decision-making. The role focuses on leveraging advanced analytics and AI to translate complex medical data into strategic decisions, ensuring scientific rigor and compliance.

Pfizer

On-site Permanent

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, defining statistical strategies, ensuring appropriate methodologies, and collaborating with cross-functional teams. They also manage outsourcing operations, represent Biostatistics in regulatory interactions, and support innovation in clinical trial design and analysis.

CSL

On-site Permanent

Director Biostatistics - Hematology

The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...

CSL

(Fixed Term) Laboratory Technician, Clinical Biomarker Laboratory, Immunoassay

The Laboratory Technician will support the Immunoassay group by executing experimental work, maintaining the lab, and ensuring high-quality data for clinical trials. The role involves hands-on lab work, preparing reagents, conducting assays, and maintaining compliance with safety and regulatory guidelines.

Moderna

On-site Contract

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and contribute to the development of regulatory processes and procedures.

Moderna

On-site Permanent

Regulatory Affairs Intelligence Director

This role involves translating regulatory intelligence into strategic decisions that accelerate drug development and improve patient outcomes. You will work closely with senior leaders to anticipate regulatory shifts, shape external policy, and convert complex data into actionable insights.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Senior Director, CGR Agentic AI Innovation

Lead the development and deployment of agentic AI systems within AstraZeneca’s Centre for Genomics Research to transform scientific workflows in genomics, multi-omics, and translational research. Translate cutting-edge AI advances into practical solutions that accelerate drug discovery and clinical decision-making by collaborating with scientists, clinicians, and engineers. Drive innovation through rapid prototyping, external partnerships, and mentorship across the R&D ecosystem.

AstraZeneca Cambridge, United Kingdom

Hybrid Permanent

Senior Principal Statistician

This role involves leading statistical strategy and innovation in clinical trial design for oncology drug development. You will apply advanced methodologies including Bayesian techniques, simulations, and risk assessment to support trials from early to late phases. Collaboration with cross-functional teams is central to enabling data-driven decisions in a dynamic R&D environment.

GSK

Hybrid Permanent

Senior Principal Statistician

This role involves leading statistical strategy and innovation in oncology clinical development, designing and analyzing trials from early to late phases using advanced methods like Bayesian statistics. The statistician will collaborate with cross-functional teams, develop analysis plans, and apply simulations to assess trial risk and success probabilities, playing a key technical and strategic role in drug development programs.

GSK

Hybrid Permanent

Senior Principal Statistician

This role involves leading statistical support for oncology clinical trials across all phases, from early development to late-stage trials. The Senior Principal Statistician will apply advanced methodologies including Bayesian techniques, simulations, and innovative trial designs to inform decision-making and assess program risk. Collaboration with cross-functional teams is central to designing studies, developing analysis plans, and ensuring robust statistical input into drug development.

GSK

Hybrid Permanent

Molecule Steward

This role involves providing end-to-end technical leadership for a pharmaceutical product across its lifecycle, from development through commercial manufacturing. The Molecule Steward ensures product quality, manufacturability, and regulatory compliance by leading cross-functional teams, defining control strategies, and driving continuous improvement initiatives across the global supply chain.

GSK United States

Hybrid Permanent

Manager, Managed Access, Oncology

Manager, Managed Access, OncologyThis position will be offered on a 15-month contractLocation – GSK LondonJoin GSK's Medical Affairs team and be part of a global organization that drives innovation, scientific excellence, and patient-centered solutions. At GSK, we are committed to...

GSK United Kingdom