Latest Medical Devices Jobs

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading clinical development strategy for oncology, specifically lung cancer, providing medical oversight across trial design, safety monitoring, and data interpretation. The Senior Medical Director will guide cross-functional teams, engage with external experts, and contribute to regulatory submissions, ensuring patient-centred, scientifically rigorous development. Based in the UK with hybrid working, the position plays a key leadership role in advancing GSK’s oncology pipeline.

GSK Stevenage, United Kingdom PLN 593,250 – PLN 988,750 pa

Senior Medical Director, Oncology Clinical Development - Lung

This role involves leading clinical development in oncology, with a focus on lung cancer, providing medical oversight across study design, execution, and data interpretation. The Senior Medical Director will guide safety monitoring, contribute to regulatory interactions, and mentor junior medical staff within a global matrix team. The position emphasizes strategic input, external scientific engagement, and integration of clinical insights to advance therapies for high unmet need.

GSK Switzerland

Hybrid Permanent

Senior Clinical Development Medical Director

This role involves providing clinical leadership and strategic medical input for cardiovascular/stroke drug development programs, including designing and executing global clinical trials. The Senior Clinical Development Medical Director will act as the global medical lead, interpreting clinical and safety data, contributing to regulatory submissions, and collaborating with cross-functional teams and external stakeholders. The position plays a key role in shaping clinical strategy and ensuring patient safety across the development lifecycle.

Novartis

Translational Medicine Expert – Dermatology, Associate Director

This role involves providing medical and scientific leadership in translational medicine for dermatology programs, spanning early to late-stage drug development. The expert will design and implement strategies for clinical pharmacology, biomarker development, and regulatory submissions, while leading cross-functional teams and supporting in-licensing opportunities. Work includes oversight of clinical studies, publication strategy, and engagement with regulatory and external stakeholders.

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

Hybrid Permanent

Bioinformatics Engineer

The role involves building and maintaining scalable bioinformatics data infrastructure and workflow orchestration systems to support plant science research. You will develop Nextflow pipelines, ETL processes, and reproducible workflows that integrate omics data from lab instrumentation into analysis-ready formats. Collaboration with bioinformaticians, data analysts, and systems administrators ensures solutions meet evolving research needs in a high-performance computing and cloud environment.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Bioinformatician - Pathogen

This role involves developing and refining bioinformatics workflows to analyse whole genome and metagenomic sequencing data for infectious disease diagnostics. The bioinformatician will work closely with wet lab scientists to interpret complex datasets, focusing on taxonomic classification, antimicrobial resistance prediction, and strain characterisation. The position supports a translational research initiative aiming to deploy scalable diagnostic tools globally.

Ellison Institute of Technology Oxford, United Kingdom

Hybrid Permanent

Director, Portfolio Development Process & Standards Lead

Lead the development and governance of processes, standards, and SOPs for CSL's global Portfolio Development function, ensuring high-quality clinical program execution. Drive cross-functional process improvement initiatives, change management, and training curriculum development. Collaborate with leadership and stakeholders across R&D to streamline decision-making and enhance operational excellence in a dynamic biotech environment.

CSL US$250,000 – US$280,000 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 area opportunities, from Phase 2 through marketed drugs. Responsibilities include engaging with Key Opinion Leaders, driving due diligence, and shaping the portfolio through high-impact partnerships.

CSL United States US$263,000 – US$328,000 pa

Hybrid Permanent

Security Engineering Manager, London or Lausanne

As a Security Engineering Manager, you will lead and scale a high-performing team responsible for securing Isomorphic Labs' AI-driven drug discovery platform. You'll define the technical security roadmap across cloud infrastructure, IAM, secure SDLC, and security monitoring, while enabling rapid innovation for ML researchers and drug discovery teams. The role involves pioneering AI-first security architectures, leading transformational projects, and acting as a key liaison within the Alphabet/Google ecosystem.

Isomorphic Labs United Kingdom

Specialist Biomedical Scientist - Infectious Sciences

This role involves performing and interpreting routine and specialist biomedical investigations in infectious sciences, including bacteriology, virology, mycology, and molecular diagnostics, within a high-volume accredited laboratory. The scientist will rotate across disciplines, lead in a designated specialty area such as quality or IT, and provide training and technical advice. Based in Taunton, the position supports a large-scale pathology service delivering over 11 million tests annually with advanced automation and 24/7 operations.

Synlab Taunton, Somerset, TA1 1HP, United Kingdom £39,959 – £48,117 pa

Mechanical Design Engineer

This role involves designing and delivering bespoke pharmaceutical process equipment and systems, ensuring compliance with strict regulatory standards. Responsibilities include conducting site surveys, producing detailed drawings, and collaborating with multidisciplinary teams to ensure integrated system functionality.

Rise10 Recruitment Leicestershire, United Kingdom £40,000 – £50,000 pa

Hybrid Permanent

Postdoctoral Immunologist

Conduct and develop immunological assays such as MSD, ELISpot, and ELISA to evaluate malaria vaccine immunogenicity in human clinical trials, primarily within the IMMUSERV project across Burkina Faso and The Gambia. Analyse data, contribute to publications, and support junior staff within a research team focused on pre-erythrocytic malaria vaccines at the Jenner Institute.

University of Oxford Oxford, South East England, United Kingdom £39 – £47 pa

Contract

Senior Safety Scientist / Associate Director / Director

This role involves leading pharmacovigilance and safety science activities across Roche’s medicine portfolio, with responsibilities spanning signal detection, risk management, and safety reporting. The individual will contribute to clinical development strategies, oversee post-market safety assessments, and ensure compliance with global regulatory standards. Working within a hybrid model in Welwyn, the position requires strong scientific analysis, leadership, and cross-functional collaboration in a regulated environment.

Roche Welwyn Hatfield, United Kingdom

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

Leads clinical development for assigned assets in Internal Medicine, serving as the primary clinical accountability point within Pfizer's Research & Development. Designs and oversees global clinical trials, regulatory submissions, and cross-functional team coordination, with potential involvement in obesity-related late-stage programs. Engages with external stakeholders and ensures compliance with scientific, regulatory, and safety standards.

Pfizer England

On-site Permanent

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

This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with a focus on obesity-related therapies. The Global Development Lead will design and oversee global clinical trials, create development plans, and ensure regulatory compliance across regions including China and Japan. The position requires cross-functional leadership, engagement with external stakeholders, and contribution to regulatory submissions and product labeling.

Pfizer England £214,900 – £358,100 pa

On-site Permanent