Latest Medical Devices Jobs

Clinical Development Medical Director - Cardiovascular

This role involves leading clinical development for cardiovascular assets within GSK's Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and execute clinical development plans, provide medical oversight, and collaborate across functions to advance translational and clinical studies. The position emphasizes scientific leadership, regulatory engagement, and strategic input to bring innovative medicines to patients.

GSK

Hybrid Permanent

Clinical Development Senior Medical Director - Vascular

Lead clinical development for vascular programs across early and late-phase trials, designing studies and translational plans to advance medicines for cardiovascular disease. Collaborate with cross-functional teams to shape clinical strategies, ensure regulatory compliance, and drive patient-focused innovation within GSK’s R&D pipeline.

GSK

(Senior) Group Leader, Nitrogen Fixation - Plant Biology Institute

Lead a flagship research programme in biological nitrogen fixation, focusing on engineering novel nitrogen-fixing systems in plants using metabolic and protein engineering. Recruit and manage a high-performing research team, drive translational science from lab to field, and collaborate across EIT’s interdisciplinary ecosystem. The role emphasizes rigorous experimental design, stage-gated research delivery, and the development of commercially viable, impact-driven plant science solutions.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

(Senior) Group Leader, Advanced Genome Technologies - Plant Biology Institute

Lead a flagship research programme in advanced genome technologies and next-generation plant transformation, focusing on novel DNA/RNA delivery, plant regeneration, and high-throughput engineering. Build and manage an interdisciplinary team within a newly established, rapidly scaling plant sciences institute, driving scientific innovation from lab to real-world impact. Collaborate across AI, automation, and commercialisation teams to translate breakthroughs in plant biotechnology into scalable, sustainable solutions.

Ellison Institute of Technology Oxford, United Kingdom

On-site Permanent

Specialist, R&D Contracts & Business Operations

This role supports R&D contract management and business operations within a global biopharmaceutical organization. The specialist will handle end-to-end contract processes including drafting agreements, managing purchase orders, ensuring compliance, and maintaining accurate records. Collaboration with cross-functional teams is essential to track obligations, ensure timely approvals, and promote operational efficiency in a hybrid working environment.

CSL

Hybrid 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 therapeutics. The Global Development Lead serves as the primary clinical accountability point, designing and executing global clinical development plans, regulatory submissions, and cross-functional team leadership. The position requires deep expertise in endocrinology or chronic weight management and extensive experience in Phase 1-3 clinical trials, translational medicine, and regulatory strategy across global markets.

Pfizer United States £214,900 – £358,100 pa

On-site Permanent

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

This role leads clinical development for assigned assets in Internal Medicine within Pfizer's R&D division, with accountability for designing and executing global clinical development plans. The individual will guide cross-functional teams through trial design, regulatory submissions, and lifecycle management, while serving as a therapeutic expert and strategic partner across internal and external stakeholders. Emphasis is placed on innovation, patient engagement, and compliance with global regulatory standards.

Pfizer £214,900 – £358,100 pa

On-site Permanent

Senior Manager, Clinical Operations - FSP Resource & Vendor Management

Leads the strategic planning and management of FSP (Functional Service Provider) resources within Clinical Operations, ensuring optimal resourcing, vendor performance, and cost efficiency across clinical trial functions. Acts as the primary liaison between Clinical Operations and FSP vendors, driving data-informed workforce models, financial oversight, and compliance. Works closely with Procurement/Outsourcing Excellence to align vendor contracts and governance with operational needs while supporting audit readiness and process improvement.

CSL US$170,000 – US$201,000 pa

Hybrid Permanent

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and deliver model-informed drug development (MIDD) strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize clinical trial design, dose selection, and regulatory submissions. Work across multidisciplinary teams to advance GSK’s oncology pipeline using quantitative approaches including exposure-response modeling, disease progression models, and simulation-based trial design. Drive innovation through external collaborations, publications, and adoption of cutting-edge methodologies in clinical pharmacology.

GSK

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead and execute model-based drug development strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize dose selection, trial design, and regulatory submissions. Drive innovation in clinical pharmacology through cross-functional collaboration and external engagement. Operate in a science-driven environment focused on accelerating the development of novel cancer therapies.

GSK US$188,100 – US$313,500 pa

Director, AI/ML MIDD Oncology Clinical Pharmacology, Modeling and Simulation

Lead clinical pharmacology and modelling & simulation efforts for oncology drug development, applying AI/ML and quantitative methods to optimise dosing, trial design, and regulatory strategy. Drive innovation in model-informed drug development across small molecules, biologics, and antibody-drug conjugates. Collaborate with cross-functional teams to accelerate therapies to patients using advanced pharmacometric and machine learning techniques.

GSK £188,100 – £313,500 pa

Manager, Oncology Regulatory Strategy

This role involves leading and implementing regional regulatory strategies for oncology products in the Rest of World (ROW) region, ensuring alignment with global objectives and commercial goals. The individual will represent the region on the Global Regulatory Strategic Team, manage submissions and approvals, and shape interactions with health authorities. A key focus is ensuring compliance while influencing the regulatory environment to accelerate patient access to medicines.

Pfizer Marlow, United Kingdom

Manager, Oncology Regulatory Strategy

Leads regional regulatory strategy for oncology products across the Rest of World (ROW), ensuring alignment with global objectives and timely submissions to health authorities. Works closely with cross-functional teams and external agencies to shape regulatory pathways, influence policy, and secure commercially viable labeling. Focuses on compliance, risk mitigation, and strategic engagement in a dynamic regulatory environment.

Pfizer Sandwich, United Kingdom

Manager, Oncology Regulatory Strategy

Lead regional regulatory strategy for oncology products across the Rest of World (ROW) region, aligning with global teams to ensure timely submissions, approvals, and commercially favorable labeling. Partner with project teams and health authorities to shape regulatory positions and influence the regional environment. Ensure compliance and effective implementation of regulatory standards throughout the product lifecycle.

Pfizer United Kingdom