Latest Pharmaceuticals Jobs

Senior Computational Biologist – Target ID

This role involves leading the integration of multi-omic and patient data to identify novel therapeutic targets at scale. The senior computational biologist will guide data science teams in building biologically grounded, semi-automated discovery pipelines, using advanced statistical methods to establish causal links between targets and patient outcomes. The position emphasizes translating complex biological data into actionable drug discovery insights with real-world impact.

Recursion United Kingdom US$151,800 – US$230,000 pa

Hybrid Permanent

Senior Data Platform Engineer

Your work will change lives. Including your own.Recursion is a leading, clinical-stage TechBio company decoding biology to industrialize drug discovery. Central to its mission is the Recursion Operating System (OS), a platform built across diverse technologies that continuously expands one...

Recursion United Kingdom

Manager, Labelling Strategy and Development

Lead the development and maintenance of global product labelling, including datasheets, prescribing information, and patient leaflets, ensuring accurate scientific and medical content across international markets. Collaborate with cross-functional teams in regulatory, clinical, safety, and governance to support product lifecycle management and compliance. Mentor team members, maintain documentation in regulatory systems, and contribute to labelling strategy in a complex global environment.

GSK Stevenage, United Kingdom

Hybrid Permanent

Executive Director, External Strategy & Science Advocacy

This role involves leading the external engagement and policy advocacy for GSK's Development Sciences, working with regulatory bodies, industry consortia, and academic institutions to shape the future of pharmaceutical innovation. Key responsibilities include developing policy strategies, advancing technical capabilities, and building strategic partnerships.

GSK United States

On-site Permanent

Scientist – Peptide Chemistry

This role involves conducting laboratory-based experimental work in peptide chemistry, designing and synthesizing peptides using solid-phase techniques, and contributing to the development of new peptide medicines. The position offers opportunities for personal and professional growth within a dynamic and collaborative team.

AstraZeneca Cambridge, United Kingdom

On-site Permanent

Process Engineer - Drug Substance Manufacture (DSM)

This role involves optimizing chemical manufacturing processes for drug substances in a regulated pharmaceutical environment. The engineer will lead process improvements, scale-up projects, and technology transfers while ensuring compliance with safety, quality, and environmental standards. Work includes root-cause analysis, change control management, and cross-functional collaboration to enhance capacity, robustness, and efficiency in API production.

AstraZeneca Macclesfield, United Kingdom

Hybrid Permanent

Global Labelling Director (Team Lead), Content

This role involves leading a team of labelling professionals, developing global labelling strategies, and ensuring compliance with regulatory requirements. The Director will collaborate with cross-functional partners and drive continuous improvement in labelling processes.

Novartis London, United Kingdom

Hybrid Permanent

Director, Evidence Generation

This role involves leading the scientific oversight of global evidence generation studies, from Phase IIIb/IV trials to real-world evidence programmes. You will develop and implement integrated evidence strategies, influence product medical strategy, and engage with global stakeholders, including key opinion leaders and patient organisations.

Novartis London, United Kingdom

Hybrid Permanent

Steriles Business Change Lead

Lead business change initiatives for sterile manufacturing at a GSK site in Barnard Castle, ensuring operational readiness across quality, compliance, and production systems. Coordinate cross-functional teams through commissioning, validation, and go-live phases, with a focus on safety, regulatory compliance, and sustainable performance improvement in a highly regulated pharmaceutical environment.

GSK Barnard Castle, United Kingdom

On-site Permanent

Associate Director, Diagnostic Planning Lead - Oncology

This role leads diagnostic planning initiatives within GSK’s Oncology Translational Medicine team, coordinating cross-functional efforts across clinical development, regulatory, and external partners to advance diagnostic assets. The position ensures alignment of project timelines, manages risks, and supports regulatory submissions, leveraging expertise in biomarkers and in vitro diagnostics within an oncology context.

GSK United States US$151,500 – US$252,500 pa

Hybrid Permanent

Associate Director, Diagnostic Planning Lead - Oncology

This role leads diagnostic planning initiatives within GSK’s Oncology Translational Medicine team, coordinating cross-functional projects and external partnerships to advance biomarker and diagnostic development. The position ensures alignment across clinical, regulatory, and commercial stakeholders, manages timelines and budgets, and supports regulatory submissions. It requires expertise in diagnostics, project management, and oncology drug development.

GSK US$151,500 – US$252,500 pa

Hybrid Permanent

ViiV Healthcare (GSK) Clinical Development Director

The Clinical Development Director at ViiV Healthcare will lead the scientific strategy and direction of clinical development programs, ensuring high-quality and timely studies. This role involves collaborating across various teams to design and finalize study protocols, provide scientific oversight, and ensure regulatory compliance. The position is crucial for advancing ViiV's mission to improve the lives of people living with HIV through innovative treatments and community support.

GSK

On-site Permanent

ViiV Healthcare (GSK) Clinical Development Director

The Clinical Development Director at ViiV Healthcare will lead the scientific strategy and execution of clinical development programs for HIV treatments. This role involves designing and overseeing high-quality clinical studies, collaborating with cross-functional teams, and ensuring regulatory compliance and safety monitoring. The position offers a unique opportunity to contribute to groundbreaking HIV research and make a significant impact on patient lives.

GSK United States

On-site Permanent

ViiV Healthcare (GSK) Clinical Development Manager

The Clinical Development Manager at ViiV Healthcare provides scientific leadership and direction for clinical development programs, focusing on the design and execution of high-quality studies. This role involves collaborating with cross-functional teams to ensure study protocols meet strategic objectives, overseeing data collection and analysis, and contributing to regulatory reporting and scientific outputs.

GSK United States

On-site Permanent

ViiV Healthcare (GSK) Clinical Development Manager

The Clinical Development Manager at ViiV Healthcare is responsible for providing scientific leadership and direction in the design and development of high-quality clinical studies. This role involves collaborating with cross-functional teams to ensure the accuracy and timeliness of study results, contributing to regulatory reporting, and creating scientific outputs for publications and presentations.

GSK

On-site Permanent