Latest Technology Jobs

GSK logo

Medical Director - Oncology Clinical Development

The Medical Director will lead the development of oncology treatments, collaborating with a multidisciplinary team to design and execute clinical trials from early to late stages. Responsibilities include medical oversight, protocol development, safety monitoring, and strategic partnerships with key stakeholders.

GSK
Hybrid Permanent
GSK logo

Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, focusing on advancing the development of antibody drug conjugates (ADCs) for solid tumors. Key responsibilities include collaborating with multidisciplinary teams to design and execute clinical trials, ensuring high-quality protocol development, and engaging with key external experts to drive data generation and regulatory approvals.

GSK
Hybrid Permanent
Pfizer logo

Director, Medical Insights

The Director, Medical Insights role at Pfizer involves shaping and implementing Medical Insights processes, collaborating with various stakeholders, and leveraging advanced analytics and AI to translate complex medical data into actionable insights. The role focuses on embedding these insights into medical decision-making and strategic discussions, ensuring they are relevant and impactful across Pfizer’s portfolio of medicines.

Pfizer
Remote Permanent
Pfizer logo

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing strategies to enhance Pfizer's medical insights capabilities. Key responsibilities include developing insights frameworks, driving alignment across medical affairs, and leveraging advanced analytics and AI to translate complex data into actionable insights that inform strategic decisions.

Pfizer
On-site Permanent
CSL logo

Associate Director, Regulatory Project Manager

This role leads global regulatory project planning and execution across CSL’s biologics product portfolio, overseeing end-to-end regulatory submissions and cross-functional collaboration. The individual will manage project timelines, risk, and compliance while driving process improvements and mentoring junior staff. Work involves close coordination with regulatory, clinical, manufacturing, and policy teams to meet global health authority requirements.

CSL US$170,000 – US$210,000 pa
Hybrid Permanent
CSL logo

Associate Director, Biostatistics (2)

The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, ensuring appropriate methodologies for study design, data analysis, and regulatory submissions. They collaborate with cross-functional teams, manage outsourcing operations, and represent Biostatistics in regulatory interactions.

CSL United Kingdom
On-site Permanent
AstraZeneca logo

Senior Tax Manager – Tax Reporting and UK Tax Compliance

Senior Tax Manager – Tax Reporting and UK Tax ComplianceLocation: Cambridge, London or Luton UKAbout AstraZenecaAstraZeneca is a global, innovation-driven biopharmaceutical business that focuses on the discovery, development and commercialization of prescription medicines for some of the world's most serious...

AstraZeneca Chatham, ME4 4NP, United Kingdom
Moderna logo

Senior Project Specialist, Clinical Supplies

This role involves managing end-to-end clinical supply operations for Moderna’s mRNA-based therapies, ensuring investigational products are labeled, packaged, and distributed efficiently and in compliance with regulatory standards. The specialist coordinates with CROs, vendors, and internal teams to maintain supply chain continuity, troubleshoot logistics, and support digital innovation in supply systems, including AI-enabled tools and IRT platforms.

Hybrid Permanent
Moderna logo

Sr. Engineer, Process Automation

The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.As Moderna continues to expand its presence in Harwell, this role...

AstraZeneca logo

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
GSK logo

Product Director, Molecule Design Products

This role leads the product strategy for AI-powered molecule design solutions within GSK’s R&D division, focusing on accelerating drug discovery through Generative AI, LLMs, and autonomous agents. The director will modernize legacy tools, build foundational data capabilities, and shape human-AI interaction for scientists, ensuring seamless integration into existing research workflows.

GSK Stevenage, United Kingdom
Hybrid Permanent
GSK logo

Product Director, Molecule Design Products

Lead the strategic development and modernization of AI-powered molecule design products to accelerate drug discovery at GSK. Define product vision, drive adoption of Generative AI and autonomous agents, and lead a team of product managers to deliver transformative tools for scientists. Ensure integration with cloud-native infrastructure and responsible AI practices across the R&D lifecycle.

GSK London, United Kingdom
Hybrid Permanent
GSK logo

Senior Director, Portfolio Integration Lead - Hematology

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-asset thought leader, shaping disease-level strategies, biomarker approaches, and trial designs while collaborating with senior teams and external experts. It emphasizes portfolio coherence, data-driven decision-making, and clinical trial innovation within a matrix environment.

GSK Stevenage, United Kingdom US$242,250 – US$403,750 pa
Hybrid Permanent
GSK logo

Global Study Manager

The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget are met. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Central Study Team to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.

GSK United Kingdom
Hybrid Permanent