Jobs in Leeds

Antibody Discovery Scientist

This role involves leading the design and execution of experiments for antibody and protein discovery, using yeast-based and phage display platforms, in silico design tools, and other innovative technologies. The scientist will work in a lab-centric environment, contributing to the development of therapeutic antibodies and proteins, and collaborating with matrix teams on various disease targets.

GSK Stevenage, Hertfordshire, United Kingdom

Antibody Discovery Associate Scientist

This role involves working in a lab-centric environment, focusing on antibody discovery and engineering using yeast-based and phage display platforms, combined with in silico design tools. The position offers opportunities to develop skills in molecular biology, AI-driven protein design, and collaboration within a dynamic team of experts.

GSK Stevenage, Hertfordshire, United Kingdom

Clinical Quality and Compliance Lead

The Clinical Quality and Compliance Lead is responsible for ensuring compliance with quality standards, regulations, and guidelines for Ipsen's clinical trials. Key responsibilities include building quality plans, identifying and managing compliance risks, supporting clinical operations, and ensuring audit and inspection readiness. The role requires strong communication, leadership, and problem-solving skills.

Ipsen London, Greater London, United Kingdom

Senior Regulatory Affairs Consultant - Labelling Strategy (home or office based)

This role involves developing and maintaining labeling strategies for pharmaceutical products, including the creation and management of core data sheets, US Prescribing Information, and EU Summary of Product Characteristics. The Senior Consultant will collaborate with various stakeholders to ensure global alignment and compliance, and contribute to clinical study designs and regulatory strategies.

Parexel Harrow, Greater London, United Kingdom

Remote

Process Technician 11-Month

Operate and monitor manufacturing processes in a cGMP-regulated biopharmaceutical environment, supporting the production of life-changing medicines. Perform troubleshooting, contribute to process improvements using Lean methodologies, and assist in validation and documentation activities. Work within a rotating shift pattern in a safety-focused, highly regulated team setting.

Appcast Enterprise Dublin, County Dublin, IV17 0YF, Ireland

Contract

Biostatistician II

As a Biostatistician II, you will lead and advise on the statistical aspects of clinical trials, developing and executing complex analysis strategies. You will collaborate with cross-functional teams, review statistical reports, and ensure high-quality deliverables, contributing to the development of new therapies.

Parexel Harrow, Greater London, United Kingdom

Remote

Senior Director, Medical Strategy Lead- Cardiology /Endocrinology / Nephrology (Obesity)

The Senior Director, Medical Strategy Lead provides strategic medical and scientific expertise in Cardiology, Endocrinology, and Nephrology, particularly in Obesity. Responsibilities include leading proposal development, participating in client meetings, and formulating clinical development plans. The role involves significant collaboration and thought leadership within the organization.

IQVIA Reading, Berkshire, United Kingdom

Remote Permanent

FSP Principal Medical Writer (Regulatory) - Client-Dedicated

The role involves writing and editing clinical study reports, protocols, and other complex scientific documents. The Principal Medical Writer will lead a team, provide training, and ensure compliance with regulatory requirements and best practices.

Thermo Fisher Scientific Remote, United Kingdom

Clinical Program Director Early Development Oncology

The Clinical Program Director (CPD) for Early Development Oncology leads the global operational delivery of oncology programs, managing a team of Clinical Project Managers, Clinical Monitoring Leads, and Clinical Trial Assistants. The role involves driving clinical partnerships, ensuring compliance with regulations, and fostering a culture of collaboration and excellence.

Ipsen London, Greater London, United Kingdom

Global Research Program Manager

The Global Research Program Manager will drive internal operational efficiency, coordinate cross-team projects, manage key partnerships, and oversee the tools and operations that the technical teams rely on. This role involves optimizing processes, facilitating collaboration, and ensuring that the team can focus on pioneering research and development.

Basecamp Research London, Greater London, United Kingdom

On-site Permanent

Enterprise Process Expert - Clinical Quality - 24 Month Secondment

This role involves supporting the development and deployment of future state clinical quality processes within AstraZeneca's global ERP transformation program. The focus is on leveraging SAP S/4 HANA capabilities to standardize and optimize end-to-end processes, ensuring compliance with regulatory standards and improving business outcomes.

AstraZeneca Macclesfield, Cheshire East, United Kingdom

Contract

Undergraduate Clinical Development Scientist

This role involves supporting the clinical development of vaccines through various activities, including protocol development, regulatory compliance, data review, and medical oversight. The position provides hands-on experience in a busy clinical research environment, contributing to global vaccine programs and promoting STEM activities.

Pfizer Marlow, Buckinghamshire, United Kingdom

Global Site and Study Operations Contracting Undergraduate

This role involves hands-on experience in clinical site contracting, including drafting and negotiating contracts with clinical trial sites and investigators. The candidate will work closely with an experienced team lead, gaining insights into legal terms, budget concepts, and regulatory requirements. There are also opportunities to support process improvement and other functions within Global Site and Study Operations (GSSO).

Pfizer United Kingdom - Sandwich

Sr Director, Medical Writing

The Senior Director, Medical Writing role involves leading and managing a team of medical writers, overseeing the creation of complex regulatory submissions, and collaborating with cross-functional teams to ensure high-quality document delivery. The position requires significant experience in life sciences and a strong background in regulatory affairs.

Gilead Sciences Cambridge, Cambridgeshire, United Kingdom

Global Clinical Program Lead

The Global Clinical Program Lead role involves overseeing a significant portion of a clinical program, particularly in late-phase respiratory and immunology studies. Responsibilities include managing a team, ensuring compliance with regulations, and contributing to the strategic direction and success of clinical trials.

AstraZeneca Cambridge, Cambridgeshire, United Kingdom

Hybrid Permanent