Latest Medical Devices Jobs

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading oncology clinical development for lung cancer programmes, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director ensures patient safety, guides cross-functional teams, and represents the programme in regulatory and scientific forums. Based on-site with a future relocation to Cambridge, UK, the position emphasizes strategic clinical leadership within a global biopharma environment.

GSK

On-site Permanent

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading oncology clinical development for lung cancer programmes, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director ensures patient safety, contributes to regulatory engagements, and mentors medical teams within a cross-functional environment. The position integrates physician expertise into clinical strategy and external scientific forums, focusing on advancing care in high unmet need cancers.

GSK

On-site Permanent

Laboratory Technician - Plant Biology Institute

This role involves hands-on support for plant science research, including cultivating experimental plants under controlled conditions, preparing reagents and media, performing molecular biology techniques like protein extraction and Western blotting, and maintaining sterile tissue cultures. The technician will assist in Agrobacterium-mediated transformations, microbial and plant cell culture, and operate bioreactors, while ensuring rigorous lab maintenance, accurate data recording, and compliance with biosafety and GMO protocols. The position is central to enabling high-throughput, scalable research within a multidisciplinary team focused on sustainable agriculture and plant-based innovation.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Glassware and Media Prep Technician - Plant Biology Institute

This role involves preparing and sterilising culture media and laboratory solutions, cleaning and maintaining glassware, and operating autoclaves and related equipment to support plant biology research. The technician ensures compliance with safety and regulatory standards while maintaining accurate records and managing consumable stock levels. Their work enables smooth laboratory operations and high-quality scientific outcomes in a cutting-edge research environment.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Senior Director, Search & Evaluation Late TA Lead, Immunology

Lead the strategic sourcing and evaluation of late-stage therapeutic assets in Immunology, Hematology, or related areas, from Phase 2 through marketed drugs. Drive cross-functional due diligence, engage with key opinion leaders and clinical networks, and shape portfolio strategy through high-impact partnerships and transactions. Operate within a global biotech ecosystem with strong collaboration across R&D, BD, and regulatory functions.

CSL US$263,000 – US$328,000 pa

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 US$263,000 – US$328,000 pa

Hybrid Permanent

Associate Director, Statistical Programming

Lead a global team of statistical programmers, driving standardization, innovation, and quality in clinical trial data analysis. Develop programming strategies using modern tools like R, Git, and AI-enabled technologies, ensuring audit-ready deliverables and alignment with biostatistics and data management. Provide technical leadership and influence global drug development strategy across phases I–IV studies.

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

Hybrid Permanent

Global Program Safety Lead - CRM

This role involves leading the end-to-end safety strategy for priority pharmaceutical programs in the Cardio Renal Metabolism (CRM) therapeutic area, from development through lifecycle management. The individual will serve as the scientific safety leader, driving safety governance, benefit-risk assessments, and regulatory interactions, while mentoring teams and embedding safety insights across global functions. It requires deep expertise in pharmacovigilance, cross-functional leadership, and clear communication of complex safety data.

Novartis London, United Kingdom £83,510 – £155,090 pa

Study Manager, Clinical Operations

Manages end-to-end clinical trial operations for 2–3 gene therapy studies, ensuring compliance with global regulatory standards and internal SOPs. Coordinates cross-functional teams, CROs, and vendors to deliver on timelines and budget, with responsibilities spanning protocol development, site selection, data integrity, and risk management. Focuses on patient safety, trial documentation, and operational planning within a rare disease gene therapy context.

Orchard Therapeutics London, United Kingdom

Hybrid Permanent

Global Development Lead, Internal Medicine, Sr. Director (MD)

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with end-to-end accountability for creating and executing global clinical development plans. The position requires deep therapeutic expertise in chronic weight management or endocrinology, leadership of cross-functional teams, and active engagement in trial design, regulatory submissions, and lifecycle strategy. The role operates in a hybrid work model and may include responsibilities across the Obesity portfolio.

Pfizer United States £274,500 – £457,500 pa

On-site Permanent

Director, HTA, Value & Evidence (HV&E), Obesity Early Pipeline

Lead the development and execution of global health economics and outcomes research (HEOR) strategies for obesity and internal medicine products in early clinical development. Design and oversee real-world evidence studies, economic modeling, and patient-reported outcomes to support market access and reimbursement. Collaborate with cross-functional teams and external stakeholders to ensure evidence generation aligns with global payer and regulatory requirements.

Pfizer United States

Pharmaceutical Manufacturing Technician

Prepare and compound sterile pharmaceutical products including total parenteral nutrition and chemotherapy in a cleanroom environment, following strict GMP and SOPs. Focus on accuracy, aseptic technique, and timely delivery of life-saving medicines to hospitals. Work within a supportive team with opportunities for accreditation-based progression and a 4-day week shift pattern.

ITH Pharma Middlesex, London, United Kingdom £30,073 pa

Associate Director, Safety Epidemiology – Global Patient Safety

Lead the design and execution of post-authorisation safety studies using real-world data to assess and communicate the safety profiles of AstraZeneca’s medicines. Provide strategic epidemiological input to regulatory submissions, safety signal evaluations, and diversity initiatives, collaborating with internal teams and external partners. Drive methodological excellence in pharmacoepidemiology and contribute to global patient safety decision-making across a broad product portfolio.

AstraZeneca Chatham, ME4 4NP, United Kingdom

On-site Permanent

Engineering Manager

The Engineering Manager (Shift) leads a multiskilled team responsible for maintaining pharmaceutical equipment and utility systems in a GMP-regulated manufacturing environment. This role involves overseeing reactive and planned maintenance, managing contractors, conducting risk assessments, and ensuring compliance with GDP, ALCOA, and GMP standards. The position operates on rotating shifts and requires strong leadership, problem-solving, and technical expertise in cleanroom operations and controlled systems.

Autolus Stevenage, United Kingdom

Senior Scientist, R&D

Develops and optimizes metagenomic extraction and sequencing workflows for diverse sample types, focusing on low-biomass and inhibitor-rich matrices. Works end-to-end from DNA/RNA extraction to library prep, with emphasis on high molecular weight recovery and virology applications. Collaborates globally to enhance data quality and scalability for AI-driven biological discovery.

Basecamp Research London, United Kingdom

On-site Permanent