Future Tech Jobs
Future Tech Jobs
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...
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 Biomedical Scientist (BMS) role involves performing analytical testing, operating and maintaining laboratory equipment, and processing patient samples in Blood Sciences disciplines. Responsibilities include result authorisation, quality assurance, and supporting patient care through collaboration with clinical and laboratory teams.
Leading provider of industrial sensor solutions are looking for a Sales Engineer - Sensors coming from a mechanical or electrical background. This is a field-based sales role covering East England, Northeast England, and Scotland, focused on driving B2B technical sales...
Job summaryWe have an exciting opportunity for a Specialist Biomedical Scientist in Clinical Biochemistry/Immunology. The service supports all hospital wards and departments, as well as GPs, clinics, and private hospitals across central and south Buckinghamshire and beyond. The central laboratory...
As a Specialist Biomedical Scientist in Haematology and Blood Transfusion, you will work across central and satellite laboratories, processing and analysing patient samples, performing complex tests, and maintaining high standards of quality and safety. You will also support junior staff, manage stock, and participate in out-of-hours duties.
About LM ManufacturingLM Manufacturing is a leading generic pharmaceutical manufacturer based in Weedon, Northamptonshire (NN7 4PP), specialising in the production of multi-use liquid pharmaceutical bottles. Our MHRA and FDA-approved facility operates to the highest standards of quality, compliance, and patient...
This role involves developing and validating analytical methods for APIs, authoring and maintaining ASMFs, and supporting regulatory submissions. The chemist will work closely with cross-functional teams, manage method transfers, and ensure regulatory compliance for pharmaceutical ingredients.
The Clinical Trials Associate will manage Trial Master File (TMF) activities, ensuring compliance and inspection readiness. Responsibilities include coordinating documentation, supporting study start-up and close-out, and assisting with site visits and data management.
The Senior Specialist I, QA Clinical is responsible for quality oversight in clinical development, supporting cross-functional relationships and ensuring compliance with GCP/GVP regulations. Key responsibilities include developing and implementing risk-based audit plans, conducting audits, and managing quality events. The role involves working closely with clinical project teams and external stakeholders, and maintaining the quality management system.
The Medical Director, Oncology Clinical Development will lead clinical research activities for GSK’s oncology portfolio, collaborating with various stakeholders to develop and execute phase 1-3 clinical trials. Key responsibilities include protocol development, medical monitoring, safety data review, and strategic partnerships with key external experts.
The Research Technician role involves developing and evaluating next-gen chromatography media, supporting method optimisation experiments, and performing analytical testing for membrane chromatography products. The position is part of the Fibro R&D department and focuses on monoclonal antibody purification workflows.
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.
This role involves leading the calibration, maintenance, and repair of medical devices to ensure they meet regulatory standards. You will work both in the field and at the Oxford site, managing audits, approving certificates, and building strong client relationships. The position offers a mix of technical, customer-facing, and leadership responsibilities, with a focus on continuous improvement and staying up-to-date with medical technologies.
The role involves managing the procurement, stock control, and stock rotation of medicines and medical devices, supervising daily stock checks, and supporting staff development and training. You will also assist with audits, medicines reconciliation, and the implementation of pharmacy procedures, working closely with the pharmacy manager and wider hospital team.
In this role, you will manage the end-to-end execution of clinical trial registration and results posting, ensuring Roche complies with global regulations. You will lead the accurate and timely posting of clinical trial data, manage cross-functional teams, and ensure consistency and quality in all submissions.
