Future Tech Jobs
Future Tech Jobs
The Role:Joining Moderna means advancing mRNA science to transform medicine. Work with exceptional global teams on a broad pipeline and build a career that makes a real difference for patients.As Moderna continues to expand its presence in Harwell, this role...
The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and clear communication. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory compliance and process improvement.
The Principal Medical Writer will lead the creation of high-quality clinical and regulatory documents, working closely with cross-functional teams to ensure scientific rigor and compliance. This role involves strategic planning, project management, and translating complex data into clear narratives, with a focus on regulatory submissions and process improvements.
The Research Pipeline Project Manager will lead and coordinate cross-functional pre-clinical research projects, partnering with scientists and clinical teams to advance scientific priorities. Responsibilities include end-to-end planning, risk management, and driving improvements in project delivery processes, with a focus on patient impact and team collaboration.
The Laboratory Technician will support the Immunoassay group by executing experimental work, maintaining the lab, and ensuring high-quality data for clinical trials. The role involves hands-on lab work, preparing reagents, conducting assays, and maintaining compliance with safety and regulatory guidelines.
This role involves developing and implementing CMC regulatory strategies for global submissions, providing guidance on regulatory CMC aspects, and ensuring compliance with health authority guidelines. The candidate will support multiple programs in various therapeutic areas, including vaccines, oncology, and rare diseases, and contribute to the development of regulatory processes and procedures.
The Head of DMPK will lead the DMPK strategy, ensuring scientific excellence and robust human dose projections. You will collaborate with data science and ML teams to refine predictive ADME models, support external partnerships, and develop a high-performing team.
Lead a team of computational biologists to integrate multi-omics data for oncology target discovery and validation, while actively contributing to analyses and mentoring team members. Drive biomarker strategy and patient stratification to advance precision oncology programs. Collaborate closely with biologists, chemists, and clinical teams to deliver data-driven insights that accelerate drug development.
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 leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA submissions, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.
This role focuses on strengthening the operational and data foundations for Supported Studies at GSK, ensuring data integrity, system performance, and compliance. The Associate Director will lead digital integration, dashboard governance, and process improvements, acting as a bridge between business and technology teams to enhance efficiency and regulatory adherence in clinical operations.
This role leads operational excellence for Supported Studies at GSK, focusing on data integrity, system governance, and digital transformation. The individual will own the data and dashboard ecosystem, act as Business System Owner for key platforms like IdeaPoint and Veeva, and ensure compliance with regulatory requirements such as Transfer of Value. They will bridge business and technology to drive process improvements, enable resource planning, and enhance data transparency across clinical operations.
This role focuses on strengthening the operational and digital foundations of GSK's Supported Studies program. The Associate Director will lead data governance, system ownership, and digital integration efforts, ensuring data integrity, compliance, and efficiency across platforms like Veeva and IdeaPoint. The position acts as a bridge between business and technology, driving process improvements and digital transformation in a regulated clinical environment.
This role leads the operational and digital foundations for Supported Studies at GSK, ensuring data integrity, system performance, and compliance across platforms like Veeva and IdeaPoint. The individual will drive process improvements, support regulatory reporting such as Transfer of Value, and act as a bridge between business and technology teams to enhance efficiency and scalability in clinical operations.
This role involves leading the operational execution of Clinical Trial Applications (CTAs) globally, outside the US, with a focus on the UK regulatory landscape. Responsibilities include managing CTA activities, ensuring regulatory compliance, coordinating with CROs, and leveraging advanced digital tools to enhance submission efficiency.
