Future Tech Jobs
Future Tech Jobs
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.
The Project Manager for External Manufacturing-Drug Substance (EM-DS) leads technical transfer projects to external CMOs, ensuring timely and budgeted delivery. Key responsibilities include managing cross-functional teams, mitigating risks, and maintaining strong relationships with suppliers and internal stakeholders.
This role involves developing and delivering robust regulatory strategies for oncology products, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation in regulatory affairs.
We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares...
We create a place where people can grow, be their best, be safe, and feel welcome, valued and included. We offer a competitive salary, an annual bonus based on company performance, healthcare and wellbeing programmes, pension plan membership, and shares...
This role involves defining and leading the European commercial strategy for GSK’s lung oncology portfolio, ensuring alignment with global strategies and driving successful product launches across multiple European markets. Key responsibilities include performance management, cross-functional collaboration, and ensuring patient access to GSK medicines.
This role involves leading statistical strategies for key oncology programs, designing robust clinical trials, and providing technical leadership to statisticians and statistical programmers. The position emphasizes innovation, regulatory interactions, and cross-functional collaboration to drive the development of new cancer therapies.
This role involves leading statistical strategies for oncology programs, designing clinical trials, and mentoring statisticians. The position emphasizes innovation, regulatory interactions, and cross-functional collaboration to advance new cancer therapies.
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.
The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Global Study Lead to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.
The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget are met. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and collaborating with the Central Study Team to achieve study deliverables. The role emphasizes innovation, risk management, and stakeholder communication.
The Global Study Manager role involves leading the operational delivery of clinical studies from initiation to archiving, ensuring timelines, quality, and budget adherence. Key responsibilities include crafting delivery plans, leading the Operational Working Group, and ensuring compliance with ICH/GCP guidelines. The role emphasizes innovation, risk management, and stakeholder communication.
This role involves leading the scientific design and execution of interventional clinical studies in oncology or hematology, ensuring high standards of quality and ethics. You will collaborate with cross-functional teams, provide scientific oversight, and engage with healthcare professionals to deliver impactful results.
This role involves providing medical and scientific expertise in safety evaluation and risk management for GSK's clinical and post-marketing assets. Responsibilities include signal detection, data analysis, and communication of safety risks, as well as supporting safety governance and cross-functional teams.
As a Regulatory Conformance Officer, you will ensure that GSK's products meet all licensing and regulatory requirements, maintaining compliance with global market authorisations and supporting regulatory submissions. You will collaborate with multiple functions, including manufacturing, R&D, and global regulatory affairs, to deliver regulatory strategies and inspection readiness.
