Latest Healthcare 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

Sales Account Manager - Diagnostics

As a Sales Specialist in Tissue Diagnostics, you will lead the sales strategy and execution for Roche's Cellular Pathology products, working with key stakeholders in the NHS and private sectors. You will manage complex procurements, develop market insights, and expand Roche's market presence in the North UK region.

Roche United Kingdom

On-site Permanent

Global Study Lead

The Global Study Lead is responsible for managing the full lifecycle of clinical studies, from design and planning to execution and documentation. Key responsibilities include leading the study team, ensuring compliance with regulations, managing budgets, and collaborating with cross-functional teams and external partners to deliver high-quality study results.

Roche United States

On-site Permanent

Associate Director, CMC Regulatory Science, International

This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and contribute to the development of regulatory processes and procedures.

Moderna

On-site Permanent

Associate Director, Global Regulatory Science, CMC

Lead global CMC regulatory strategy for mRNA medicines, guiding international submissions and ensuring compliance with health authority requirements. Collaborate with manufacturing and quality teams to support product development across vaccines, oncology, and rare diseases. Develop and maintain regulatory documentation in CTD format, while driving process improvements and change control assessments.

Moderna

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards. You will act as a primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios and leading cross-functional discussions to resolve quality issues.

Novartis Ireland

Hybrid Permanent

Senior Scientific Engagement & Program Manager

This role involves planning and executing high-quality medical and scientific engagement activities across various therapeutic areas, including Oncology, Cardiovascular Disease, and Immunology. The Senior Scientific Engagement & Program Manager will coordinate advisory boards, congress activities, and medical education programs, ensuring seamless delivery and continuous improvement in processes and tools.

Novartis London, United Kingdom

Hybrid Permanent

Field Service Engineer, Laboratory Automation Systems

This role involves installing, servicing, repairing, and calibrating advanced laboratory automation and diagnostics systems used in NHS and clinical laboratories. The engineer will work on-site at customer locations, supporting complex equipment such as flow cytometry and cell separation systems, with a strong focus on technical problem-solving and customer support. The position requires weekend work on a rotating basis, with time off in lieu.

TRS Consulting Chelmsford, Essex, United Kingdom £52,000 pa

On-site Permanent

Field Service Engineer, Laboratory Automation Systems

Provide on-site technical service, installation, repair, and calibration of advanced laboratory automation and diagnostics systems in healthcare environments. Support complex instrumentation for pathology and clinical chemistry labs, with a focus on customer-facing problem resolution and preventative maintenance. Work involves periodic weekend coverage and travel to client sites.

TRS Consulting Sutton, London, United Kingdom £52,000 pa

On-site Permanent

Senior Software Engineer (Platform)

As a Senior Software Engineer at Owkin, you will design, implement, and maintain cloud-based infrastructure and services that support complex biomedical research and business intelligence. You will own critical platform components, drive technical standards, mentor junior engineers, and collaborate with cross-functional teams to enhance productivity and security.

Owkin United Kingdom

Remote Permanent

Associate Field Technical Engineer

Trainee / Associate Clinical Specialists - Electrophysiology (x2)Great Graduate Opportunities within Medical DevicesLocations: 1x South West England | 1x MidlandsSalary: £34,000 per annum + 30% personal performance bonusBenefits: £580 monthly car allowance (or company car scheme) + fantastic benefits packageContract:...

Randstad Engineering Bristol, Bristol (county), United Kingdom

Associate Field Technical Engineer

Trainee / Associate Clinical Specialists - Electrophysiology (x2)Great Graduate Opportunities within Medical DevicesLocations: 1x South West England | 1x MidlandsSalary: £34,000 per annum + 30% personal performance bonusBenefits: £580 monthly car allowance (or company car scheme) + fantastic benefits packageContract:...

Randstad Engineering Birmingham, West Midlands (county), United Kingdom

Medical Sales Representative

Medical Sales Representative – Respiratory DiagnosticsA global company that has led the way in the development and manufacture of respiratory ventilation products for 65+ years. With a reputation for delivering excellent clinical outcomes and a genuine ethical approach to business...

Progress Sales Recruitment Leicester, Leicestershire, United Kingdom £45,000 – £50,000 pa

Senior Process Engineer

The Senior Process Engineer role at AstraZeneca involves developing and scaling up sustainable drug substance manufacturing processes. Responsibilities include introducing new equipment, optimizing processes, and collaborating with cross-functional teams to ensure robust and efficient production for clinical and preclinical trials.

AstraZeneca Macclesfield, United Kingdom

On-site Permanent