Latest Innovation Jobs

Statistics Director, Oncology

This role involves leading statistical strategies for key oncology programs, designing robust clinical trials, and mentoring statisticians. The position emphasizes innovation, regulatory interactions, and cross-functional collaboration to advance the development of new cancer therapies.

GSK Stevenage, United Kingdom

On-site Permanent

NIS P&D Study Delivery Lead, Associate Director

The NIS P&D Study Delivery Lead, Associate Director, is responsible for leading the full lifecycle of clinical studies and trials within the Non-Interventional Study (NIS) portfolio. This includes designing, executing, and reporting complex regulatory commitment studies, managing team members, and ensuring compliance with regulatory guidelines. The role also involves leading operational decision-making, risk management, and driving innovation in study delivery through new technologies.

GSK Stevenage, United Kingdom £87,000 pa

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Worthing, United Kingdom

Hybrid Permanent

Project Manager (EM-DS - External Manufacturing-Drug Substance)

The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMO partners, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.

GSK Barnard Castle, United Kingdom

Hybrid Permanent

Head of RTSM (Randomization and Trial Supply Management)

This role involves leading the RTSM function, 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, ensuring on-time randomization and supply availability, and improving RTSM processes and governance.

GSK Stevenage, United Kingdom

Hybrid Permanent

Operational Quality Director

The Operational Quality Director at GSK will lead the end-to-end quality oversight of manufacturing activities, ensuring compliance with GMP standards and regulatory requirements. Key responsibilities include managing batch documentation, overseeing real-time quality control, and leading the QP team to maintain high-quality standards and inspection readiness.

GSK East Hertfordshire, United Kingdom

On-site Permanent

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

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

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

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

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

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

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

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

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