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 Global Study Lead is responsible for overseeing the design, planning, execution, and documentation of clinical studies, ensuring compliance with regulatory requirements and delivering high-quality results within budget and timelines. The role involves leading cross-functional teams, collaborating with internal and external stakeholders, and managing study-level budgets and operational aspects.
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.
This role involves evaluating current clinical assay performance monitoring methods and designing a digital solution to improve standardization and visibility across laboratory teams. The intern will work with real datasets and collaborate with scientists to prototype tools for tracking assay performance, potentially incorporating AI-driven insights. The position offers hands-on experience in a regulated clinical environment and cross-functional stakeholder engagement.
This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading regulatory discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.
This role involves providing expert Good Clinical Practice (GCP) compliance guidance to clinical trial teams, supporting decision-making on complex regulatory issues, leading quality issue resolution, and ensuring inspection readiness across global clinical programs. The manager will translate regulatory requirements into actionable insights, conduct self-assessments, and drive continuous improvement in compliance. Embedded within cross-functional teams, the role emphasizes proactive risk mitigation, data integrity, and collaboration with Quality Assurance and Development functions.
This role involves leading the global medical affairs strategy for oncology, shaping early portfolio decisions, and ensuring evidence plans meet stakeholder needs. Responsibilities include developing medical plans, generating innovative evidence, and building partnerships with healthcare professionals and scientific leaders.
This role involves installing, servicing, repairing, and calibrating advanced laboratory automation and diagnostics systems in NHS and clinical environments. The engineer will work on-site at customer locations, supporting complex equipment such as flow cytometry and cell separation systems. The position requires strong technical expertise in electro-mechanical systems and excellent customer-facing skills.
This role involves installing, servicing, repairing, and calibrating advanced laboratory automation and diagnostics systems in clinical and NHS environments. The engineer will work on-site with complex electro-mechanical systems, providing technical support and breakdown resolution for critical healthcare equipment. The position requires strong field service skills and direct customer interaction in high-pressure settings.
This role involves leading and influencing strategic decisions in AstraZeneca's Oncology Global Programme Management, focusing on TDR, DDR, and Epigenetics. You will guide comprehensive programme strategies, connect various stages of drug development, and ensure optimal portfolio delivery.
This role involves leading the bioanalytical strategy for diverse therapeutic modalities, collaborating with global project teams to develop robust assays, and translating complex data into clear program decisions. The position is highly visible, requiring cross-functional influence and external representation of scientific findings.
Your work will change lives. Including your own.The Impact You'll MakeRecursion is reimagining drug discovery through the integration of automated cell biology, high-dimensional data, and AI-driven analytics. As Head of Strategy & Operations, you will be our CEO's closest strategic...
