Latest Medical Devices Jobs

Senior CMC Regulatory Strategy Manager

Leads CMC regulatory strategy for pharmaceutical development and lifecycle management, coordinating technical submissions and advising on global regulatory requirements. Works cross-functionally to ensure compliance, support inspections, and maintain product supply. Focuses on risk mitigation, process improvement, and influencing regulatory decisions across complex projects.

GSK London, United Kingdom £90,000 – £150,000 pa

Hybrid Permanent

Director, DP Workstream Leader – Small Molecule Parenteral (LAIs and Oligos)

This role involves leading late-stage drug product development for sterile long-acting injectables and oligonucleotides, overseeing formulation, process development, and technology transfer across clinical and commercial phases. The position acts as a strategic bridge between CMC project teams and functional execution, ensuring regulatory robustness, supply readiness, and integrated solutions through cross-functional leadership. It emphasizes scientific excellence, risk mitigation, and patient-focused innovation within a hybrid working model.

GSK United States

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 drive value and impact across Pfizer’s medical portfolio.

Pfizer United States

On-site Permanent

Director, Medical Insights

The Director, Medical Insights role involves shaping and implementing processes to generate and apply high-quality medical insights across Pfizer. Key responsibilities include developing Medical Insights strategies, prioritizing use cases, translating complex data into actionable insights, and embedding these insights into core medical processes to support informed decision-making and strategic discussions.

Pfizer London, SW7 2AP, United Kingdom

Hybrid Permanent

Senior Clinical Trial Leader - Translational Medicine

This senior role involves leading the scientific and operational aspects of complex, global early phase clinical trials. Responsibilities include designing and delivering high-quality studies, leading cross-functional teams, and ensuring robust data for key portfolio decisions. The role requires strong scientific and leadership skills, with a focus on continuous improvement and team collaboration.

Novartis London, United Kingdom

Hybrid Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic assets, engaging with key opinion leaders, and integrating innovation into portfolio planning. The position requires deep clinical expertise, a proven track record in deal-making, and strong collaboration with cross-functional teams.

CSL £263,000 – £328,000 pa

Hybrid Permanent

Director, Portfolio Development Process & Standards Lead

This role leads the establishment and maintenance of processes and standards across CSL's global Portfolio Development function, ensuring high-quality clinical trial planning, evaluation, and reporting. The Director will drive process improvement, SOP governance, training curriculum development, and cross-functional change initiatives within a dynamic biotech R&D environment. They will work closely with leadership and international teams to reduce complexity, improve quality and speed, and align procedural frameworks across clinical development, biomarkers, and commercial operations.

CSL

Hybrid Permanent

Associate Director, Statistical Programming

This role leads statistical programming efforts across global clinical trials, managing teams and driving innovation in data analysis and visualization. The individual will shape programming strategy, ensure audit readiness, and collaborate with cross-functional teams to deliver high-quality statistical outputs. Emphasis is placed on adopting modern tools like R, Shiny, and Git for reproducible, standardized workflows in drug development.

Novartis London, United Kingdom £67,900 – £126,100 pa

Hybrid Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include mentoring regulatory professionals, partnering with directors on global strategies, and representing the Global Regulatory Affairs function in senior interactions and health authority meetings.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Executive Regulatory Science & Strategy Director, Oncology

This role involves leading the Hematology group within Oncology Regulatory Affairs, providing strategic regulatory expertise and oversight for the development and commercialization of oncology products. Responsibilities include coaching regulatory leads, partnering on global strategies, leading resource planning, and representing the function in senior interactions and health authority meetings.

AstraZeneca United States

On-site Permanent