Latest Pharmaceutical Scientist Jobs

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

Field Service Engineer, Medical Diagnostic Systems

This role involves servicing and repairing advanced medical diagnostic and laboratory systems used in NHS and private healthcare settings. The engineer will conduct on-site maintenance, perform breakdown repairs, and provide technical troubleshooting support to laboratory staff. Full product training is provided, emphasizing customer service and technical reliability in a high-stakes clinical environment.

TRS Consulting Southampton, Hampshire, SO19 8NJ, United Kingdom £52,000 pa

On-site Permanent

Field Service Engineer, Medical Diagnostic Systems

Install, maintain, and repair advanced medical diagnostic systems in NHS and private laboratory settings. Provide on-site technical support, troubleshoot complex instrumentation, and deliver high-quality customer service during service and breakdown calls. Work independently across a defined region with comprehensive training and support.

TRS Consulting Gloucester, Gloucestershire, United Kingdom £45,000 – £48,000 pa

On-site Permanent

Vaccines Safety Sciences Lead

Leads and manages pharmacovigilance and safety sciences functions, ensuring compliance with global regulatory standards and GxP guidelines. Oversees signal detection, safety data analysis, and regulatory documentation such as the PSMF, while driving process improvements and supporting PV inspections. Acts as a strategic expert in implementing safety systems and translating business requirements into technical solutions for global teams.

CSL

Hybrid Permanent

Associate Director, Global Regulatory Science, CMC

Leads global regulatory strategy for CMC (Chemistry, Manufacturing, and Controls) in support of mRNA-based medicines, ensuring compliance with international regulations and guiding submissions across multiple therapeutic areas. Works closely with manufacturing, quality, and development teams to prepare high-quality regulatory documentation and engage with health authorities. Focuses on biologics, particularly in vaccines, oncology, and rare diseases, within a rapidly expanding biotech environment.

Moderna London, United Kingdom

Hybrid Permanent

Executive Regulatory Science Director, Respiratory & Immunology

Lead global regulatory strategy for respiratory and immunology therapies across development stages, from early research to commercialization. Provide expert guidance on regulatory pathways, engage with health authorities, and mentor regulatory leaders. Shape policy and ensure compliance while advancing innovative treatments through key milestones and approvals.

AstraZeneca

Associate Director, Global Regulatory Science, CMC

This role leads global regulatory CMC strategy for mRNA-based medicines, developing and implementing regulatory plans for international submissions. The individual will guide CMC documentation, interact with health authorities, and provide strategic input across product development stages, ensuring compliance with EU and global regulations. The position plays a key part in advancing Moderna’s pipeline of transformative therapeutics across vaccines, oncology, and rare diseases.

Moderna

Hybrid Permanent

Senior Specialist - Quality Assurance (Night shift)

This role involves providing Quality Assurance leadership on the night shift for aseptic manufacturing and packaging operations, ensuring compliance with GMP and internal standards. The specialist will oversee cleanroom practices, manage deviations and change controls, support product release, and coach manufacturing staff on cGMP and contamination control. It plays a critical part in maintaining regulatory compliance and patient safety within a lean, science-driven environment.

AstraZeneca Macclesfield, United Kingdom

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

Sr. Manager, RWE/EPI Internal Medicine

This role involves leading real-world evidence and epidemiological research to support Pfizer's Internal Medicine portfolio across the drug development lifecycle. The individual will design and deliver global studies, synthesize data into actionable insights, and collaborate with cross-functional teams and external partners. Emphasis is placed on scientific rigor, regulatory engagement, and leveraging data sources including AI tools to inform medical strategy.

Pfizer

Sr. Manager, RWE/EPI Internal Medicine

Lead the design and execution of real-world evidence and epidemiological studies to support Pfizer's Internal Medicine portfolio. Synthesize scientific literature, develop study protocols, and deliver insights from observational data to inform global medical strategy and regulatory submissions. Collaborate across functions and with external partners to advance the use of RWE in drug development.

Pfizer

Investor Relations and Business Development Associate

Supports fundraising campaigns for life sciences and healthcare companies by building relationships with investors and stakeholders. Coordinates investor engagement, maintains CRM records, and contributes to investor communications and market intelligence. Works across multiple campaigns to drive successful outcomes through data-led outreach and stakeholder coordination.

Equals One M502St, M50 2ST, United Kingdom £35,000 – £40,000 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, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while guiding cross-functional teams and managing vendor performance. They also support redaction of confidential information and drive process improvements across disclosure operations.

CSL United Kingdom

Operations Lead

Lead end-to-end manufacturing, logistics, and warehouse operations within a regulated life sciences environment, driving performance in safety, quality, delivery, and cost. Champion lean principles and continuous improvement while developing teams and supporting new product introductions and site expansion initiatives.

Hays Procurement Jobs Llantrisant, Mid Glamorgan, United Kingdom £75,000 – £85,000 pa

On-site Permanent