Future Tech Jobs
Future Tech Jobs
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.
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.
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.
This role involves leading the global health outcomes function at ViiV Healthcare, focusing on evidence generation to support HIV treatment and prevention medicines. Responsibilities include strategic leadership, team management, and collaboration with various stakeholders to ensure credible and decision-relevant evidence for patient access and value demonstration.
This role involves leading the global health outcomes function at ViiV Healthcare, designing and delivering robust evidence to support HIV treatment and prevention medicines. Responsibilities include strategic leadership, evidence generation, and collaboration with various stakeholders to optimize patient access and value demonstration.
The SERM Scientific Director role involves leading pharmacovigilance and risk management strategies for clinical development and post-marketing products. Responsibilities include evaluating safety data, managing safety concerns, and supporting regulatory activities. The role operates in a global, cross-functional environment and may include mentoring responsibilities.
This role involves developing and delivering robust regulatory strategies for drug development and approval, collaborating with cross-functional teams, and ensuring compliance with global regulatory requirements. The position also focuses on process improvement and innovation within the regulatory framework.
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...
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.
This role involves leading a global matrix programme team to transform incoming material testing and data management across GSK's manufacturing sites. Responsibilities include defining future-state operating models, creating global standards, partnering with ERP and LES teams, and ensuring data integrity and regulatory compliance.
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.
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.
