Latest Life Sciences 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

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 compliance. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory submissions and process improvements.

GSK

On-site Permanent

Director, Clinical Trial and Data Transparency

This role involves providing strategic and operational expertise for the disclosure of clinical regulatory documents on public websites, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes and technologic solutions to support transparency in clinical trials.

Pfizer India

Remote Permanent

Director, Clinical Trial and Data Transparency

This role involves leading the strategic and operational aspects of clinical trial transparency and disclosure, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes for compliance.

Pfizer

Remote Permanent

Research Scientist (Applied LLMs), London

This role involves advancing drug discovery by applying Large Language Models to complex biological and chemical challenges. The Research Scientist will develop and refine LLM-driven methods, collaborate with interdisciplinary teams, and contribute to cutting-edge AI models that accelerate scientific breakthroughs. The position emphasizes innovation in model architecture, post-training techniques, and real-world application of AI in computational biology.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Research Scientist (Machine Learning), London

A Research Scientist in Machine Learning will develop novel deep learning models and algorithms to advance drug discovery at Isomorphic Labs. Working in an interdisciplinary environment, the role involves designing AI architectures, training models on biological and chemical data, and collaborating with scientists to solve complex problems in digital biology. The work directly contributes to building a cutting-edge AI-driven drug design engine.

Isomorphic Labs London, United Kingdom

Hybrid Permanent

Senior Scientist – AI and Computational Tools, Oncology R&D (12-Month

This role involves designing and deploying AI-powered tools and workflows for oncology research, building robust data infrastructure, and mentoring colleagues in computational methods. The Senior Scientist will work closely with wet-lab scientists, data science teams, and R&D IT to translate experimental data into scalable, reproducible systems.

AstraZeneca Cambridge, United Kingdom

On-site Contract

Medical Director, Senior Patient Safety Physician

This role involves leading clinical safety strategy for drug projects across development and post-marketing phases, with a focus on oncology. The Medical Director will evaluate safety data from clinical and pre-clinical sources, contribute to global regulatory submissions, and guide risk management using advanced methodologies like signal detection and Safety Knowledge Groups. Based in Luton with a hybrid working model, the position drives patient safety within a global, science-led environment.

AstraZeneca Chatham, ME4 4NP, United Kingdom

Hybrid Permanent Flexible

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with internal and external teams to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and supplies.

GSK Stevenage, United Kingdom

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working closely with internal and external teams to ensure studies are delivered on time, on budget, and in compliance with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK Poland

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Key responsibilities include monitoring study conduct, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key documents, coordinating meetings, managing communications, and overseeing clinical supplies and budget tracking.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are on time, on budget, and compliant with standards. Responsibilities include monitoring study progress, drafting key clinical documents, coordinating meetings, managing study communications, and overseeing clinical supply and investigational product delivery.

GSK

Hybrid Permanent

Study Manager

The Study Manager role involves leading and coordinating clinical and evidence generation studies, working with study teams, vendors, and country colleagues to ensure studies are delivered on time, on budget, and compliant with standards. Key responsibilities include monitoring study progress, drafting clinical documents, coordinating meetings, and managing study communications and budgets.

GSK

Hybrid Permanent