Latest Pharmaceutical Scientist Jobs

Cardio-Renal Discovery Disease Area Lead

The Discovery Disease Area Lead for Cardiovascular-Renal Diseases at GSK will lead the identification and validation of therapeutic targets for chronic kidney disease, glomerulonephritis, and cardiovascular conditions. You will manage a cross-functional team, drive scientific excellence, and collaborate with external experts to translate human disease phenotype information into actionable therapeutic innovations.

GSK Stevenage, United Kingdom

Cardio-Renal Discovery Disease Area Lead

The Discovery Disease Area Lead for Cardiovascular-Renal Diseases at GSK will lead the identification and validation of therapeutic targets for chronic kidney disease, glomerulonephritis, and cardiovascular conditions. You will manage a cross-functional team, drive scientific excellence, and collaborate with external experts to translate human disease phenotype information into actionable therapeutic innovations.

GSK

Medical Insights, Data Analyst Senior Manager

This role involves conducting ad hoc and exploratory data analysis to answer complex business and medical questions that cannot be addressed through existing platforms. The Senior Manager partners with global Medical Insights teams to translate ambiguous queries into actionable analytical approaches, validate datasets, and deliver clear, decision-ready insights. A key differentiator is the protected time for innovation—testing new data sources, AI methods, and proof-of-concept analyses to inform the strategic evolution of Pfizer’s global analytics platform.

Pfizer United States US$124,400 – US$207,400 pa

Medical Insights, Data Analyst Senior Manager

Performs ad hoc and exploratory data analysis to address complex business and medical questions that existing platforms cannot answer. Translates ambiguous queries into analytical approaches, validates datasets, and delivers clear, decision-ready insights to stakeholders in Medical Affairs. Also pilots new data sources, methods, and AI-driven techniques to inform future platform development and roadmap priorities.

Pfizer US$124,400 – US$207,400 pa

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing advanced medical diagnostic systems in NHS and private laboratory settings. The engineer will troubleshoot on-site, provide technical support, and liaise with laboratory staff. Full product training is provided, and the role requires some weekend work due to a five-day-in-seven schedule.

TRS Consulting Livingston, West Lothian, EH54 6GS, United Kingdom £52,000 pa

Field Service Engineer, Medical Diagnostic Systems

Perform installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratories. Provide on-site technical support and troubleshooting, working closely with lab staff across diverse healthcare settings. Role includes extensive field work with full product training provided.

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

On-site Permanent

Global Safety Lead - Formulation Safety

Leads global safety strategy for formulation safety within CSL's GSPV department, overseeing clinical safety evaluation across product lifecycles. Responsible for signal detection, risk management planning, and regulatory compliance across clinical development and post-marketing phases. Serves as safety representative in cross-functional teams, ensuring alignment with medical, regulatory, and business objectives.

CSL

Associate Director, CMC Regulatory Science, International

Lead the development and execution of CMC regulatory strategies for mRNA-based products across global submissions, including IND/CTA/BLA/MAA filings. Provide expert guidance on regulatory compliance, interact with health authorities, and support quality and manufacturing teams through change controls and submissions. Work within a multidisciplinary team at the Harwell site to advance Moderna’s pipeline in vaccines, oncology, and rare diseases.

Moderna London, United Kingdom

On-site Permanent

Associate Director, CMC Regulatory Affairs, International

This role involves leading CMC regulatory strategies and submissions for international markets, with a focus on mRNA-based products across vaccines, oncology, and rare diseases. The individual will guide global regulatory compliance, interact with health authorities, and support manufacturing and quality teams through regulatory interpretation and change control. It requires deep expertise in CTD-format filings and a proactive approach to managing multi-therapeutic regulatory programs in a fast-paced environment.

Moderna

On-site Permanent

GCP Compliance Director (Program & Study)

Lead a team of GCP Compliance Managers to ensure global clinical trials adhere to Good Clinical Practice and regulatory standards. Drive inspection readiness, audit oversight, and quality issue management across clinical development programs. Shape compliance strategy and foster a culture of quality and continuous improvement within a matrixed pharmaceutical environment.

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

Hybrid Permanent

GCP Compliance Director (EMEA Hub)

This role leads Good Clinical Practice (GCP) compliance across Novartis' EMEA clinical operations, ensuring trials meet regulatory, quality, and ethical standards. The director oversees audits, inspections, and compliance events, while developing a high-performing team and driving risk mitigation. They will partner with global clinical and quality leaders to strengthen inspection readiness and operational excellence in a hybrid working environment.

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

Associate Director, Clinical Trial Disclosure & Transparency

This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.

CSL

Associate Director, Clinical Supply Chain

This role involves leading the end-to-end clinical supply chain strategy for global trials, managing complex logistics, and optimizing workflows using AI. You will work closely with cross-functional teams to ensure supply strategies align with trial milestones and commercial readiness.

Recursion United Kingdom

Clinical Supply Chain Manager

This role involves leading the end-to-end clinical supply chain strategy for global trials, managing complex logistics, and optimizing data-driven workflows. You will work closely with cross-functional teams to ensure supply strategies align with trial milestones and commercial readiness.

Recursion United Kingdom

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Senior Engineer, CSV Validation

This role involves end-to-end ownership of computerised system validation (CSV) for GxP-regulated systems used in the manufacturing and testing of advanced CAR-T cell therapies. The engineer will author and execute validation documentation, ensure compliance with international regulations (e.g. FDA 21 CFR Part 11, EU GMP Annex 11), manage change controls and CAPAs, and support regulatory inspections. The position requires strong technical writing, cross-functional collaboration, and expertise in GAMP 5 and data integrity within a biopharmaceutical context.

Autolus Stevenage, United Kingdom