Hybrid Jobs in Wales, United Kingdom

Sedgwick’s Property Adjuster team in North Wales drives the resolution of domestic loss claims. The role involves visiting customers, coordinating contractors, and settling claims while maintaining detailed reports.

Biologics Analytical Research & Development team at Merck drives GMP-compliant release, stability, and in-process testing of biologic drug substances and products. The Senior Scientist validates ELISA and cell‑based potency methods, manages analytical life‑cycle, and collaborates with QA, CMC, and regulatory teams to support product launches.

Merck Oncology Market Access Insights team drives analytical strategy to optimize payer access and pricing for oncology products. The Associate Director leads end‑to‑end analytics—from data ingestion and engineering to advanced modeling and Power BI visualization—to inform senior stakeholders on coverage, reimbursement, and formulary impact.

Lead clinical development of immunology therapeutics, overseeing trial design, execution, regulatory reporting, and publication. Manage cross‑functional teams, engage investigators, and provide scientific expertise to support drug safety, efficacy, and market strategy.

Senior scientist responsible for developing and maintaining global core, US, and local labeling documents for pharmaceutical products, leading cross‑functional teams, ensuring regulatory compliance, and providing labeling expertise to regulatory affairs sub‑teams.

Leads scientific planning and execution of clinical trials in ophthalmology, guiding cross‑functional teams worldwide. Drives protocol development, data integrity, and regulatory compliance (GCP, ICH).

Senior Principal Scientist leads strategic planning and execution of late-stage clinical research in Immunology, overseeing trial design, regulatory filing, data analysis, and publication. Manages cross-functional teams, collaborates with external experts, and supports business development.

Regulatory Affairs Manager at Cancer Research UK oversees regulatory strategy for early-phase oncology trials, manages CTA and IMPD submissions across UK and EU, leads cross-functional teams, ensures compliance with legislation, and improves regulatory processes.

Principal Scientist in Translational Oncology leading companion diagnostics and digital pathology projects, coordinating cross-functional teams, selecting assays, engaging regulatory agencies, and driving global CDx strategy.

Apprentice Corporate Bank L6 | S1 | Corporate and Commercial Banking| Multiple Locations

Clinical Quality Assurance Assistant supports the QA team in managing the Quality Management System (QMS) for Cancer Research UK's Centre for Drug Development. The role involves administering QMS tasks, user and document lifecycle management, training staff, compiling quarterly metrics, and coordinating inspection activities.

This role leads technical projects and equipment assessments in packaging and device assembly, driving process improvements, compliance, and cross‑functional collaboration across multiple sites.

Legal Counsel needed to support UK & EMEA contract negotiations, ensuring compliance and alignment with business priorities. Works remotely or from Cardiff, London, or Leeds, meeting quarterly.

Senior Director, Clinical Research, Cardiovascular and Respiratory at Merck leads planning and execution of clinical studies for new and marketed medicines in cardiovascular and respiratory therapeutic areas. Responsibilities include developing clinical strategies, designing trials, overseeing study conduct, analyzing data, and collaborating with cross‑functional teams in commercialization, regulatory affairs, statistics, and manufacturing.

The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the therapeutic area. Our company’s medicines span all phases of clinical development (pre-clinical to post-licensure).

Legal Counsel role overseeing contract negotiations across UK and EMEA, ensuring compliance and alignment with business priorities. Works remotely or from Cardiff, London or Leeds offices, meeting quarterly for team gatherings.

The Associate Principal Scientist, Clinical Research position is part of Merck’s 2‑year Physician Scientist Program, offering pharmaceutical medicine training to physicians completing residency or fellowship. Candidates will spend the first year in Global Clinical Development, Global Regulatory Affairs and Clinical Safety, or Global Medical/Scientific Affairs, gaining exposure to clinical trial planning, execution, data analysis, regulatory interactions, and product lifecycle management.

Director, Market Research at Merck leads a global team of market research professionals to design and execute research plans across the product lifecycle, framing critical business questions, integrating data sources, managing vendors, and providing strategic partnership to commercial, R&D, and medical functions. The role requires deep expertise in quantitative and qualitative research methodologies, secondary data analytics, epidemiology, and vaccine portfolio knowledge, and drives innovation and technology to modernize market research and deliver actionable insights in near real time.

Canadian Solar’s e-STORAGE subsidiary seeks a Global Risk Manager to lead risk processes across commercial operations in Canada, USA, Europe. The role drives compliance, market research, pricing strategy, and risk mitigation for BESS offerings, supporting sales and execution teams.

Consumer Services Assistant role at LexisNexis Risk Solutions UK Ltd. supports customers for Crediva, Consumer Rights, and UK Insurance. Based in Cardiff, the hybrid position requires at least two days in office.