Latest Pharmaceuticals Jobs

Principal Medical Writer

The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and clear communication. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory compliance and process improvement.

GSK United States

On-site Permanent

Principal Medical Writer

Leads medical writing for complex clinical and regulatory projects, including protocols, study reports, and submission dossiers. Translates clinical data into clear scientific narratives and acts as a subject matter expert on regulatory standards. Works cross-functionally in a fast-paced, mission-driven HIV-focused environment.

GSK

On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

A Field Service Engineer will maintain and repair advanced medical diagnostic systems in NHS and private laboratory settings, providing on-site technical support and troubleshooting. The role involves regular weekend work and extensive customer interaction with laboratory staff. Full product training is provided, emphasizing customer service and technical excellence in a high-reliability healthcare environment.

TRS Consulting Trowbridge, Wiltshire, BA14 8EY, United Kingdom £52,000 pa

On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

Perform on-site installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratories. Provide technical troubleshooting and customer support across complex clinical environments. Receive full product training and work within a globally recognised healthcare technology organisation.

TRS Consulting Southampton, Hampshire, United Kingdom £52,000 pa

Risk Surveillance Lead

The Risk Surveillance Lead drives Risk-Based Quality Management (RBQM) adoption at the trial level, overseeing risk identification, mitigation, and continuous improvement across clinical trials. This role involves facilitating cross-functional risk assessments, managing quality tolerance limits, conducting central surveillance using RBQM analytics, and leading risk review discussions. It plays a key role in ensuring clinical quality governance and compliance with GCP standards within a matrix environment.

Novartis London, United Kingdom

Hybrid Permanent

Clinical Data Strategy, Manager

This role involves leading clinical data strategy planning and execution across Translational Medicine programs, with a focus on designing fit-for-purpose data collection approaches and supporting robust decision-making. The individual will develop Data Strategy Plans, guide trial teams on data oversight, and leverage internal and external data to inform trial design—particularly in Neuroscience. The position requires deep expertise in clinical assessments, data integrity, and cross-functional collaboration in a global, fast-paced environment.

Novartis London, United Kingdom £49,140 – £91,260 pa

Hybrid Permanent

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

This role involves leading clinical development for Internal Medicine assets at Pfizer, with end-to-end accountability for designing, executing, and interpreting global clinical trials. The individual will serve as the primary clinical leader on cross-functional teams, shaping development plans, supporting regulatory submissions, and engaging with external stakeholders. A strong emphasis is placed on strategic innovation, team leadership, and therapeutic expertise in obesity and endocrinology.

Pfizer

On-site Permanent

Senior Director, Targets and Mechanisms Solutions

Leads strategic direction and AI-driven innovation for Pfizer’s Targets and Mechanisms platforms, integrating digital technologies and data pipelines to accelerate drug discovery. Oversees global teams delivering scalable, science-centric solutions across research units, with a focus on omics data, target identification, and translational biomarkers. Drives product roadmaps, ecosystem architecture, and AI adoption to support therapeutic hypothesis generation and preclinical strategy.

Pfizer United States

Director, Global Real-World Evidence & Health Outcomes Research Scientist- Hepatology

Leads the design and execution of real-world evidence (RWE) and health outcomes research to support GSK's hepatology assets across the product lifecycle. Works cross-functionally to align evidence generation with payer, regulatory, and clinical needs, ensuring robust data for market access and value-based pricing. Engages with internal teams and external experts to translate research into impactful health outcomes strategies.

GSK US$185,250 – US$339,625 pa

Director, Global Real-World Evidence & Health Outcomes Research Scientist- Hepatology

Lead the design and execution of real-world evidence and health outcomes research studies to support GSK's hepatology portfolio. Collaborate with cross-functional teams to generate robust, scientifically credible data that informs market access, reimbursement, and value-based pricing strategies. Engage with internal and external stakeholders to align research with regulatory and payer requirements across global markets.

GSK US$185,250 – US$308,750 pa

Director, Global Real-World Evidence & Health Outcomes Research Scientist- Hepatology

Leads the design and execution of real-world evidence (RWE) and health outcomes studies to support GSK's hepatology assets, ensuring robust data generation for market access, reimbursement, and patient impact. Works cross-functionally with medical, commercial, and R&D teams to align evidence strategies with global regulatory and payer requirements. Focuses on translating complex data into actionable insights for diverse stakeholders.

GSK £185,250 – £339,625 pa

Remote Permanent

Director, Global Real-World Evidence & Health Outcomes Research Scientist- Hepatology

Lead the development and execution of real-world evidence and health outcomes research to support GSK's hepatology assets. Drive strategic evidence generation aligned with regulatory, reimbursement, and market access needs, working across global teams and external partners. Focus on robust study design, data analysis, and dissemination to influence decision-making across payers, providers, and health systems.

GSK US$185,250 – US$308,750 pa

Audit Lead

Lead and develop GMP/GDP audit strategy for sterile biologics, medical devices, or small molecule manufacturing, ensuring compliance with global regulations and Pfizer standards. Conduct complex audits across internal sites and external partners, coach auditors, and drive continuous improvement in quality systems. Collaborate with cross-functional teams to assess risks, resolve findings, and prepare for regulatory inspections.

Pfizer United States US$162,900 – US$271,500 pa

Remote Permanent

Audit Lead

Lead GMP/GDP audit strategy and execution for a key technology area such as sterile biologics or medical devices across Pfizer’s global manufacturing and supply network. Conduct complex audits at internal sites and external partners, assess compliance with global regulations, coach auditors, and drive continuous improvement in quality systems. Work cross-functionally to align audit practices with emerging regulatory trends and support inspection readiness.

Pfizer London, SW7 2AP, United Kingdom US$162,900 – US$271,500 pa

On-site Permanent

Audit Lead

Lead GMP/GDP audit strategy and execution for a key technology area such as sterile biologics or medical devices within Pfizer’s global manufacturing and supply network. Conduct complex audits at Pfizer sites and external partners, ensuring compliance with global regulations and driving continuous improvement in quality systems. Provide expert coaching to auditors and collaborate across functions to address risks and enhance audit practices.

Pfizer US$162,900 – US$271,500 pa

On-site Permanent