Latest Pharmaceutical Scientist Jobs

Molecular Design Engineer

This role involves using computational and AI-driven methods to design and optimize biopharmaceuticals, particularly complex antibody formats like multispecifics. The engineer will bridge experimental and predictive teams by developing in silico risk-scoring systems, interpreting structural data, and delivering engineered DNA constructs. The position emphasizes collaboration, data analysis, and the development of tools to support next-generation drug discovery.

GSK Stevenage, United Kingdom

Hybrid Permanent

Medical Director, Oncology Clinical Development - Hematology

This role involves leading medical oversight in oncology clinical development, focusing on hematology and clonal myeloid disorders. The Medical Director will guide study design, ensure patient safety, interpret clinical data, and collaborate with cross-functional teams and external experts. It is a physician-led position embedded in clinical strategy with a strong emphasis on real-world impact and regulatory engagement.

GSK Stevenage, United Kingdom PLN 455,250 – PLN 758,750 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

Global Safety Lead - Formulation Safety

Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...

CSL

Director, Regulatory Affairs

Lead global regulatory strategy and execution for drug development programs, ensuring compliance across jurisdictions including the US, EU, and UK. Collaborate with cross-functional teams to prepare and manage regulatory submissions such as INDs, NDAs, and orphan drug designations. Provide strategic guidance on regulatory risks and lifecycle management, while engaging with health authorities and shaping regulatory science in the context of AI-driven drug discovery.

Recursion North Tyneside, NE29 8EP, United Kingdom £207,500 – £280,720 pa

Remote 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

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

Regulatory Affairs Intelligence Director

This role focuses on transforming regulatory intelligence into strategic decisions that accelerate drug development and approvals. The individual will analyze global regulatory trends, guidance, and precedents to inform pipeline strategy and influence policy, working closely with cross-functional teams and senior leaders. Key responsibilities include conducting in-depth research, providing impact assessments, and integrating emerging technologies like AI into regulatory intelligence processes.

AstraZeneca Cambridge, 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