Latest IT Consulting Jobs

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Medical Director, Clinical Development, Immunology

We are seeking a Medical Director, Clinical Development, Immunology for a clinical program in food allergy. The Medical Director, Clinical Development, Immunology will support the Clinical Development Lead (CDL) and clinical team to plan and execute a clinical program, consisting...

GSK
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Medical Director, Clinical Development, Immunology

We are seeking a Medical Director, Clinical Development, Immunology for a clinical program in food allergy. The Medical Director, Clinical Development, Immunology will support the Clinical Development Lead (CDL) and clinical team to plan and execute a clinical program, consisting...

GSK
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Support Engineer, London

As a Support Engineer, you will provide technical support, troubleshoot complex issues, and develop automation tools to improve efficiency. You will collaborate with other teams to resolve technical issues, manage 3rd party integrations, and contribute to the onboarding of new employees. This role is crucial for shaping the support strategy and driving innovation through automation.

Isomorphic Labs United Kingdom
Hybrid Permanent
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PKPD Modelling Lead, London

Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...

Isomorphic Labs London, United Kingdom
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Senior Regulatory Managers

This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams, provide regulatory advice, and support inspections and quality events. The position offers opportunities for growth through complex regulatory work and direct impact on patient health.

GSK
Hybrid Permanent
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ViiV Healthcare (GSK) Clinical Development Director

The Clinical Development Director at ViiV Healthcare will lead the scientific strategy and direction of clinical development programs, ensuring high-quality and timely studies. This role involves collaborating across various teams to design and finalize study protocols, provide scientific oversight, and ensure regulatory compliance. The position is crucial for advancing ViiV's mission to improve the lives of people living with HIV through innovative treatments and community support.

GSK
On-site Permanent
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ViiV Healthcare (GSK) Clinical Development Director

The Clinical Development Director at ViiV Healthcare will lead the scientific strategy and execution of clinical development programs for HIV treatments. This role involves designing and overseeing high-quality clinical studies, collaborating with cross-functional teams, and ensuring regulatory compliance and safety monitoring. The position offers a unique opportunity to contribute to groundbreaking HIV research and make a significant impact on patient lives.

GSK United States
On-site Permanent
GSK logo

Senior Regulatory Managers

This role involves leading Chemistry, Manufacturing and Controls (CMC) regulatory activities across development, registration, and early lifecycle stages. You will work with cross-functional teams, provide regulatory advice, and manage interactions with regulatory authorities, ensuring compliance and supply continuity.

GSK
Hybrid Permanent
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ViiV Healthcare (GSK) Clinical Development Manager

The Clinical Development Manager at ViiV Healthcare provides scientific leadership and direction for clinical development programs, focusing on the design and execution of high-quality studies. This role involves collaborating with cross-functional teams to ensure study protocols meet strategic objectives, overseeing data collection and analysis, and contributing to regulatory reporting and scientific outputs.

GSK United States
On-site Permanent
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ViiV Healthcare (GSK) Clinical Development Manager

The Clinical Development Manager at ViiV Healthcare is responsible for providing scientific leadership and direction in the design and development of high-quality clinical studies. This role involves collaborating with cross-functional teams to ensure the accuracy and timeliness of study results, contributing to regulatory reporting, and creating scientific outputs for publications and presentations.

GSK
On-site Permanent
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Head of Precision Diagnostics External Engagement

This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive successful collaborations.

GSK United States £242,250 – £403,750 pa
On-site Permanent
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Head of Precision Diagnostics External Engagement

This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive strategic alliances and complex collaborations.

GSK £242,250 pa
On-site Permanent
GSK logo

Head of Precision Diagnostics External Engagement

This senior role involves leading business development and transactions in biomarker and diagnostics for GSK's Oncology R&D. Responsibilities include negotiating deals, aligning with R&D strategy, and collaborating with internal and external stakeholders to drive successful collaborations and strategic alliances.

GSK £242,250 – £403,750 pa
On-site Permanent
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Specialist - Extractables and Leachable - MSAT EM

This role involves working with internal and external labs to ensure E&L testing is completed scientifically and compliantly. Responsibilities include conducting risk assessments, delivering technical information, and managing risk identification for biopharmaceutical manufacturing processes and packaging systems.

GSK United States £70,650 – £117,750 pa
On-site Permanent
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Specialist - Extractables and Leachable - MSAT EM

This role involves working with internal and external labs to ensure E&L testing is completed scientifically and compliantly. Responsibilities include conducting risk assessments, delivering technical information, and managing risk escalation for biopharmaceutical manufacturing processes and packaging systems.

GSK £70,650 – £117,750 pa
On-site Permanent