Jobs in Leeds

Director, Search & Evaluation Early TA Lead (Haem)

Leads strategic sourcing and evaluation of early-stage innovation in haematology, from preclinical to Phase 1 assets. Drives due diligence, shapes partnering strategies, and executes transactions in collaboration with Business Development. Embedded in the Therapeutic Area Leadership Team to influence portfolio planning and external innovation priorities.

CSL Opfikon, Bülach District, Switzerland

Data-Flow Lead

The Data-Flow Lead role at GSK involves designing and governing data-flows for the R&D division, ensuring data is trusted, reusable, and compliant. Responsibilities include translating business needs into technical requirements, developing modular data-flows, and integrating diverse data sources into a unified format.

GSK Stevenage, Hertfordshire, United Kingdom

Associate Director, Pipeline Project Management for BD

The Associate Director, Pipeline Project Management for Business Development at GSK manages R&D projects from early diligence through integration and transition to business as usual. Key responsibilities include cross-functional planning, risk management, and ensuring smooth knowledge transfer and execution of BD transactions.

GSK Grimsby, North East Lincolnshire, United Kingdom

Central Monitor (Data Surveillance Lead)

The Central Monitor (CM) is responsible for overseeing clinical trials through centralized monitoring, ensuring data quality, identifying risks, and collaborating with cross-functional teams. Key responsibilities include executing monitoring strategies, conducting data surveillance, and supporting risk management processes.

Novartis Barcelona, Catalunya, Spain

Senior International Regulatory Affairs Director

This role involves leading the international regulatory strategy for complex cell therapy programs, ensuring regional requirements are embedded in global plans. You will work closely with global product and regulatory teams, commercial and medical leaders, and policy stakeholders to accelerate patient access and drive timely approvals.

AstraZeneca Cambridge, Cambridgeshire, United Kingdom

Manager/Associate Director - Project Management

This role involves managing the osteoporosis drug discovery programme at Relation Therapeutics, coordinating across interdisciplinary teams and third-party partners. Responsibilities include strategic planning, resource allocation, risk management, and ensuring project milestones are met.

Relation Therapeutics London, Greater London, United Kingdom

Permanent

Industrial Placement Student - Regulatory Affairs (12 months)

This 12-month industrial placement in Regulatory Affairs at Vertex Pharmaceuticals offers hands-on experience in the pharmaceutical industry. The role involves preparing regulatory documents, conducting intelligence requests, and supporting the development of medicines for serious diseases, with exposure to organizational leaders.

Vertex Pharmaceuticals London, Greater London, United Kingdom

Summer Intern, Commercial Haematology

As a Summer Intern in Commercial Haematology, you will work on the commercial launch strategies for Vertex's gene editing product, gaining hands-on experience in the pharmaceutical industry. You will collaborate with industry leaders, participate in meaningful projects, and engage in mentorship and networking opportunities.

Vertex Pharmaceuticals London, Greater London, United Kingdom

Medical Strategy Lead, Oncology-Clinical Development (Centre of Excellence)

This role involves providing strategic medical and scientific input in hematology-oncology, including early customer engagement, proposal development, and support at scientific conferences. The Medical Director will act as an internal and external consultant, guiding clinical development and research projects, and maintaining awareness of the latest scientific advancements.

IQVIA Reading, Berkshire, United Kingdom

Snr Clinical Database Designer

This role involves designing and updating clinical databases, creating edit specifications, and collaborating with various stakeholders including programmers, statisticians, and client representatives. The position requires managing multiple projects, ensuring quality and compliance, and contributing to process improvements.

IQVIA Reading, Berkshire, United Kingdom

Associate Director, Safety Analysis Scientist

The role involves leading safety assessments and evaluations for pharmaceutical products, collaborating with cross-functional teams to ensure regulatory compliance and make safety-related decisions. Responsibilities include data analysis, report writing, and supporting safety management activities.

Johnson & Johnson Innovative Medicine High Wycombe, Buckinghamshire, United Kingdom

Senior Regulatory Submission Project Manager

The Senior Regulatory Submission Project Manager collaborates with cross-functional teams to plan, coordinate, and deliver high-quality regulatory submissions. Responsibilities include managing submission timelines, leading scenario planning, and ensuring compliance with regulatory requirements and internal processes.

Ipsen London, Greater London, United Kingdom

Regulatory Submission Project Manager

The Regulatory Submission Project Manager collaborates with cross-functional teams to plan, coordinate, and deliver high-quality regulatory submissions. Responsibilities include developing project plans, managing timelines, and ensuring compliance with regulatory requirements and internal processes.

Ipsen London, Greater London, United Kingdom

Product Engineer

This role involves leading the development and management of a large-scale analytical data platform, Mystra, and its AI layer, MystraAI. Responsibilities include optimizing multi-tenant ClickHouse clusters, building resilient data pipelines, and ensuring secure, multi-tenant data access. The role also involves technical leadership and mentoring a team of engineers.

Genomics London, Greater London, United Kingdom

Hybrid Permanent

Process / Equipment Engineer

The Process/Equipment Engineer provides technical support for the Bio-Vaccines Suites, ensuring equipment reliability and resolving manufacturing issues. Responsibilities include troubleshooting, leading investigations, validation, compliance, and continuous improvement initiatives.

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