Latest Technology Jobs

Clinical Research Associate

This role involves managing and monitoring clinical trial sites remotely, ensuring compliance with Good Clinical Practice and Pfizer standards. The Clinical Research Associate serves as the primary point of contact for investigator sites, conducting remote and on-site monitoring, supporting patient safety, resolving protocol issues, and driving site activation and recruitment. The position emphasizes strong collaboration with study teams and site staff to maintain data quality and regulatory compliance throughout the trial lifecycle.

Pfizer United Kingdom

Remote Permanent

Senior Clinical Research Associate II

This role involves managing and monitoring clinical trial sites to ensure compliance with Good Clinical Practice and Pfizer standards, with a focus on patient safety and data quality. The Senior Clinical Research Associate acts as the primary point of contact for investigator sites, supporting study setup, execution, and closeout while addressing protocol issues and driving recruitment. The position requires extensive interaction with site staff, cross-functional teams, and vendors, using both on-site and remote monitoring methods.

Pfizer United Kingdom

Remote 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 Biomedical Scientist

This role involves performing full blood count analysis and using LC-MS/MS to monitor clozapine and other antipsychotic medications in a specialist pathology laboratory. The scientist will manage laboratory information systems, ensure data accuracy, and maintain quality control standards. The position also includes contributing to SOP development, method improvement, and broader lab operations such as supply chain and IT support.

Reed Specialist Recruitment Hereford, Herefordshire, United Kingdom

On-site Permanent

Laboratory Scientist - In-Vitro – Preclinical

This role involves supporting in-vitro and pre-clinical studies to generate scientific data for product safety assessment and regulatory submissions. The scientist will conduct biological assays, maintain lab operations, and contribute to data analysis within a multidisciplinary research environment. Work focuses on cell biology, toxicology, and pharmacology using cutting-edge methodologies.

Hudson Shribman United Kingdom £40,000 pa

On-site Contract

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, and ensuring adherence to quality standards across global clinical programs. The manager will lead investigations into quality issues, drive inspection readiness, and translate regulatory requirements into practical actions. Collaboration with cross-functional stakeholders is central to strengthening compliance and fostering a culture of data integrity and accountability.

Novartis London, United Kingdom

Hybrid Permanent

GCP Compliance Manager - Clinical Programs & Trials

This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, leading quality issue resolution, and ensuring inspection readiness across global clinical programs. The manager will translate regulatory requirements into actionable insights, conduct self-assessments, and drive continuous improvement in compliance. Embedded within cross-functional teams, the role emphasizes proactive risk mitigation, data integrity, and collaboration with Quality Assurance and Development functions.

Novartis Ardross, Alba / Scotland, IV17 0YF, United Kingdom

Hybrid Permanent

Global Regulatory Affairs Operations Resource Planner

This role involves partnering with stakeholders to gather and validate submission planning information, ensuring efficient resource allocation for regulatory submissions. You will contribute to process improvements and deliver metrics to support leadership decisions.

Novartis London, United Kingdom

Hybrid Permanent

Biomedical Field Service Engineer

This role involves daily repair, preventative maintenance, and asset management of medical devices across multiple hospital locations. Key responsibilities include performing scheduled maintenance, completing repairs, supporting the site manager, and maintaining safe working practices and service documentation. The role requires travel to various sites and maintaining strong customer relationships.

Focus Resourcing Berkshire, United Kingdom

On-site Permanent

Biomedical Field Service Engineer

To provide daily repair, preventative maintenance, and asset management of medical devices within various hospital locations whilst ensuring outstanding customer support and building long term relationship. Please note you must be resident in the UK with full right work. Any...

Focus Resourcing Dorset, United Kingdom

Director, QA Manufacturing

This role involves leading and developing the Front Line QA function at Seqirus Liverpool, ensuring pharmaceutical quality across all products. Responsibilities include providing 24/7 QA coverage, overseeing batch review and IT systems, and ensuring compliance with regulatory requirements. The role holder may also act as a QP, certifying and releasing products to market.

CSL United Kingdom

On-site Permanent

Director of Engineering (ML Platform), London

This role involves leading the strategic direction and operational excellence of the Platform teams, which enable the training and serving of large-scale AI models in biotech. Responsibilities include defining the long-term vision, mentoring a diverse team, and ensuring robust, scalable, and developer-friendly services across multiple disciplines.

Isomorphic Labs London, United Kingdom

On-site Permanent

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

Head, PV and Regulatory QA

TheHead of Pharmacovigilance and Regulatory Quality Assurance leads the global quality and compliance function for our pharmacovigilance system. You are the independent quality authority ensuring that our end-to-end PV processes across clinical safety, regulatory affairs, and medical affairs remain compliant...

CSL

Associate Principal AI & ML Engineer – Evinova

As an Associate Principal AI & ML Engineer at Evinova, you will develop and integrate advanced algorithms and generative AI systems to optimize clinical trial design and improve drug development processes. Your role involves working with multi-source data, building production systems, and collaborating with cross-functional teams to drive impactful solutions.

AstraZeneca London, United Kingdom

Hybrid Permanent