Latest Innovation Jobs

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Machine Learning Scientist - Quantum Chemistry

This role involves developing machine learning models grounded in quantum chemistry to accelerate small-molecule drug discovery. The scientist will create physics-informed algorithms to predict molecular properties and interactions, using proprietary datasets and high-performance computing. Collaboration with computational and experimental teams ensures direct application of models in real-world drug design workflows.

Hybrid Permanent
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Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology antibody drug conjugate (ADC) portfolio, focusing on advancing the development of clinical trials from early to late stages. Key responsibilities include protocol development, medical monitoring, safety data review, and collaboration with a multi-disciplinary team of experts to ensure the scientific integrity and timely delivery of clinical trials.

GSK
Hybrid Permanent
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Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for oncology assets, specifically in genitourinary (GU) cancers, within a global biopharma environment. The Senior Medical Director will design and execute phase 1-3 trials, ensure scientific integrity of data, and collaborate with internal teams and external experts to support regulatory filings and market launches. The position requires deep expertise in oncology drug development and strong leadership in a matrixed organization.

GSK PLN 593,250 – PLN 988,750 pa
Hybrid Permanent
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Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for genitourinary (GU) oncology programs within GSK’s pipeline, with responsibility for designing and executing phase 1–3 trials, ensuring scientific integrity, and supporting regulatory submissions. The Senior Medical Director will collaborate across functions and represent GSK externally with key experts and at medical meetings, driving data generation and strategic input for innovative oncology therapies.

GSK £284,250 – £473,750 pa
Hybrid Permanent
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Senior Medical Director, Oncology Clinical Development - GU

This role involves leading clinical development for oncology, specifically genitourinary (GU) cancers, within GSK’s global portfolio. The Senior Medical Director will design and execute Phase 1–3 trials, provide medical oversight, interpret clinical data, and collaborate with internal teams and external experts to support regulatory submissions and product lifecycle management. The position requires deep expertise in GU oncology and strong leadership in a matrixed, science-driven environment.

GSK US$284,250 – US$473,750 pa
On-site Permanent
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Medical Director, Oncology Clinical Development

The Medical Director, Oncology Clinical Development, will lead clinical research activities for GSK’s oncology portfolio, collaborating with internal and external stakeholders to design and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key experts in the field.

GSK
Hybrid Permanent
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Head of RTSM (Randomization and Trial Supply Management)

This role involves leading the RTSM function in the US, partnering with clinical development, operations, quality, and external vendors to design and deliver patient-focused randomization and clinical supply solutions. Responsibilities include managing cross-functional teams, risk assessments, process improvements, and fostering collaboration across internal and external partners.

GSK United States
Hybrid Permanent
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Disease Level Partner - South Central UK

The Disease Level Partner (DLP) is responsible for implementing Roche's strategy and objectives within therapy areas, focusing on patient outcomes. Key responsibilities include deep customer engagement, gathering actionable insights, and driving positive customer experiences. The role involves leveraging resources to secure access for key customers and contributing to the development of local and national brand advocates.

Roche United Kingdom
On-site Permanent
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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 to develop regulatory strategies, prepare submissions, and provide regulatory advice, while also mentoring colleagues and improving processes.

GSK United States
Hybrid Permanent
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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 to develop regulatory strategies, prepare submissions, and provide regulatory advice, while also mentoring colleagues and contributing to process improvements.

GSK
Hybrid Permanent
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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
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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 manage interactions with regulatory authorities, ensuring compliance and supply continuity.

GSK
Hybrid Permanent
GSK logo

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