Latest Medical Devices Jobs

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Clinical Development Medical Director - Cardiovascular

Lead clinical development for cardiovascular programs within GSK’s Respiratory, Immunology & Inflammation Research Unit, driving translational and clinical strategies from early to late stages. Provide medical oversight, design clinical development plans, and collaborate across functions to deliver innovative medicines addressing unmet patient needs. Work in a hybrid model with a future relocation from Stevenage to Cambridge by 2029.

GSK Stevenage, United Kingdom
Hybrid Permanent
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Clinical Development Senior Medical Director - Vascular

Leads clinical development for vascular programmes across early and late phases, shaping study designs and clinical development plans. Works cross-functionally with translational science, regulatory, and commercial teams to advance medicines for vascular disease, with a focus on patient impact and scientific innovation. Provides medical oversight, contributes to regulatory submissions, and guides decision-making in a matrix environment.

GSK Stevenage, United Kingdom

Postdoctoral Research Fellow - Generative Biology Institute

Conduct independent, high-impact research in a multidisciplinary environment focused on engineering biology, with responsibilities including experimental design, data analysis, publication, and mentoring junior researchers. Work at the intersection of biology, technology, and engineering within a newly established, well-resourced institute pursuing transformative solutions in health, agriculture, and sustainability.

Ellison Institute of Technology Oxford, United Kingdom £40,000 pa
On-site Permanent
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Global Development Lead, Internal Medicine, Sr. Director (non-MD)

Leads clinical development for Internal Medicine assets within Pfizer's R&D organization, with end-to-end accountability for creating and executing global clinical development plans. Serves as the primary clinical point of contact across cross-functional teams and external partners, driving trial design, regulatory submissions, and lifecycle strategy. Focuses on obesity and related therapeutic areas, integrating innovation, patient engagement, and regulatory expertise to advance drug development.

Pfizer £214,900 – £358,100 pa
On-site Permanent
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Global Development Lead, Internal Medicine, Sr. Director (non-MD)

Leads clinical development for assigned internal medicine assets within Pfizer's Research & Development division, with end-to-end accountability for creating and executing global clinical development plans. Oversees cross-functional teams to design and deliver clinical trials supporting regulatory submissions, while providing therapeutic expertise in obesity and endocrinology. Engages external stakeholders and contributes to regulatory strategy, safety reporting, and product labeling.

Pfizer £214,900 – £358,100 pa
On-site Permanent
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Quality Governance & Partnership Senior Specialist

This role involves managing quality governance systems for raw materials and suppliers at GSK’s manufacturing site. The specialist ensures compliance with pharmaceutical regulations, oversees supplier quality workflows, handles change controls and audits, and maintains documentation for material specifications and supplier agreements. The position plays a key role in maintaining supply chain integrity and regulatory compliance within a highly regulated biopharma environment.

GSK Barnard Castle, United Kingdom
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Statistics Leader / Associate Director of Statistics

This role involves providing statistical leadership across oncology clinical development, from early-phase trials to regulatory submissions. The candidate will lead study design, analysis, and interpretation using advanced methods like Bayesian approaches and real-world data integration. They will collaborate with cross-functional teams to deliver robust statistical insights that inform key development decisions in a global biopharma environment.

GSK Stevenage, United Kingdom PLN 326,250 – PLN 543,750 pa
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Continuous Improvement and Digital Expert (Quality Systems) - 18-month / Secondment

This role focuses on driving continuous improvement within quality systems at a highly regulated manufacturing site, using AI, digital tools, and data analytics to optimize processes. The professional will work cross-functionally to enhance compliance, data integrity, and inspection readiness through Power BI dashboards, metrics-driven insights, and robust governance frameworks. Emphasis is placed on implementing sustainable improvements in Deviations and CAPA, change control, training compliance, and digital quality systems.

GSK Barnard Castle, United Kingdom
On-site Contract
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Director, R&D Procurement (Antibody Drug Conjugates and Biopharmaceuticals)

Leads global procurement strategy for biopharmaceuticals and antibody drug conjugates, managing a £300M R&D spend portfolio and a team of 4–6 category managers. Focuses on sourcing from CDMOs, negotiating complex contracts, and building strategic supplier relationships to accelerate GSK’s R&D pipeline. Works closely with internal stakeholders and commercial procurement to align with supply strategy and drive innovation in drug development.

GSK PLN 369,000 – PLN 615,000 pa
Hybrid Permanent
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Head of RTSM (Randomization and Trial Supply Management)

Lead the design and delivery of Randomization and Trial Supply Management (RTSM) strategies across global clinical trials, ensuring reliable supply and randomization systems for patient-focused studies. Partner with cross-functional teams and external vendors to optimize processes, ensure compliance, and support clinical trial execution from Phase I–IV. This role emphasizes leadership in process improvement, team development, and integration of RTSM within broader clinical operations.

GSK United States
Hybrid Permanent
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Clinical Programmer/Analyst

The Clinical Programmer/Analyst designs, builds, and reviews programming solutions to transform clinical and real-world data into reliable, compliant outputs. Working closely with statisticians and data scientists, the role involves developing code for data transformation, analysis, and reporting in line with CDISC standards (SDTM, ADaM) and regulatory requirements. The position supports agile delivery of high-quality datasets, tables, listings, and figures while promoting programming best practices and innovation within a collaborative, cross-functional environment.

GSK United Kingdom
Hybrid Permanent
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Director, R&D Procurement (Antibody Drug Conjugates and Biopharmaceuticals)

Leads global procurement strategy for Antibody Drug Conjugates and Biopharmaceuticals, managing a £300M R&D spend and a team of 4–6. Focuses on sourcing from CDMOs, negotiating complex contracts, and aligning with GSK’s R&D pipeline acceleration. Works closely with internal stakeholders and external partners to drive value, cost control, and innovation in drug development.

GSK United States PLN 369,000 – PLN 615,000 pa
Hybrid Permanent
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Associate Director, PBPK-PD Translational Modeling, DMPK

Associate Director, PBPK-PD Translational Modeling, DMPKDrug Metabolism and Pharmacokinetics (DMPK) | Research & Development GSK.Closing Date: 1st September 2026 (COB)Business IntroductionAt GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the...

GSK
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Global Regulatory Affairs Manager

Develops and executes global regulatory strategies for oncology products, ensuring compliance and optimal labeling across regions. Collaborates with cross-functional teams and regulatory authorities to support product development and approvals. Focuses on strategic planning, regulatory intelligence, and process innovation within a patient-first framework.

GSK United Kingdom
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Global Regulatory Affairs Manager

Develops and executes global regulatory strategies for oncology products, ensuring compliance and optimal labeling across markets. Collaborates with cross-functional teams and regulatory authorities to support product development and approvals. Focuses on innovation, patient impact, and strategic alignment within a matrix environment.

GSK
Hybrid Permanent