Future Tech Jobs
Future Tech Jobs
CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means...
The Director, Biostatistics, leads the full scope of statistical contribution to a clinical development program, including life cycle management. The AD provides for statistical excellence in clinical development plans, trial planning, data analysis, interpretation and reporting, and regulatory interactions and...
As a Clinical Study Administrator, you will coordinate and manage the administrative aspects of clinical trials, ensuring that all documentation, regulatory submissions, and stakeholder communications are accurate and timely. You will work closely with various teams to maintain inspection readiness and support the smooth operation of multi-site studies.
Work with usOur team are passionate in the pursuit of excellence and in pushing the boundaries of cancer therapy and Autoimmune disease to deliver life-changing treatments to patients.Whilst working at Autolus you will enjoy a flexible, diverse and dynamic working...
This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.
This role involves working as a technical expert in the Clinical Flow Cytometry group at Moderna's Harwell facility, focusing on generating high-quality clinical trial data through advanced flow cytometry assays. Responsibilities include executing clinical sample testing, conducting immune profiling, and ensuring data integrity and compliance with GCLP standards.
The Research Associate will work closely with the R&D and manufacturing teams to develop and optimize manufacturing processes for CAR-Treg therapies. Responsibilities include conducting experiments, managing databases, improving process design, and handling mammalian and primary human immune cell cultures. The role requires on-site presence and flexibility to travel between London sites.
The Research Associate will manage inventory, prepare reagents, and run automated systems for high-throughput screening. They will collaborate with cross-functional teams to optimize workflows and adopt new technologies, contributing to the company's drug discovery platform.
The role involves leading the analysis and interpretation of multiomic data in cardiac disease, developing data-driven approaches for population segmentation, and working with complex multi-omic datasets. You will collaborate with data scientists to build integrative models combining imaging and biological data, and contribute to writing papers using novel methods.
Your work will change lives. Including your own.The Impact You’ll MakeRecursion is at the forefront of reimagining drug discovery and development through broadening the funnel of potential targets, using technology and standardization to build connected data. As a research scientist...
This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, including medical monitoring, safety data review, and clinical data management. The position also includes mentoring others and contributing to protocol design and study strategy.
This role involves overseeing medical and scientific aspects of clinical trials in Internal Medicine, ensuring data integrity and quality. Responsibilities include medical monitoring, safety data review, protocol development, and collaboration with internal and external stakeholders.
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 Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...
The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinicaldevelopment program. The AD provides statistical strategies for the clinical trials and regulatorysubmissions, and is accountable for the statistical deliverables within the program.Lead full scope of...
This role involves leading statistical planning and delivery for clinical programs in oncology, working closely with cross-functional teams to design robust clinical trials and contribute to regulatory strategies. The position also focuses on methodological innovation and mentoring colleagues to build statistical capability and quality.
The Business Analyst will support a key programme focused on the collection, tracking, and lifecycle management of human biological samples. Responsibilities include eliciting and documenting requirements, mapping end-to-end processes, and facilitating stakeholder workshops to enhance biobanking systems and data flows.
