Future Tech Jobs
Future Tech Jobs
Leads clinical development for respiratory assets, designing and executing clinical and translational strategies to advance drug candidates. Provides medical oversight, contributes to regulatory submissions, and collaborates across functions to deliver innovative medicines. Focuses on patient-centric innovation and scientific rigor in a matrix environment.
This role involves leading clinical development for aging-related therapies within GSK’s Respiratory, Immunology & Inflammation Research Unit. The Medical Director will design and execute clinical development plans, provide medical oversight, and integrate translational and clinical data to advance drug candidates. The position emphasizes cross-functional leadership, regulatory engagement, and innovation in trial design to deliver differentiated medicines.
This role involves leading global clinical trial teams through phase 1 and 2 development, drafting early clinical development plans, and serving as a medical lead for early clinical studies. The Medical Director will collaborate with biomarker experts, research scientists, and key opinion leaders to identify and implement strategies for preclinical and clinical support of gastroenterology programs.
A Field Service Engineer will maintain and repair advanced medical diagnostic systems in NHS and private laboratory settings, providing on-site technical support and troubleshooting. The role involves regular weekend work and extensive customer interaction with laboratory staff. Full product training is provided, emphasizing customer service and technical excellence in a high-reliability healthcare environment.
Field Service Engineer, Medical Diagnostic SystemsBasic Salary Up To £50,000Overall Earnings £60,000+Bonus 15%£10 Per Day Lunch AllowanceCompany CarPensionHealthcareLife InsurancePhone, LaptopHolidaysThe Role – Field Service Engineer, Medical Diagnostic SystemsThis market leader seeks to recruit a technically motivated and customer focused Field...
This role involves leading the development and maintenance of global core labelling documents for neuroscience products, ensuring accuracy, compliance, and consistency across markets. The individual will facilitate cross-functional alignment, conduct competitor and regulatory research, and support implementation of labelling updates throughout the product lifecycle. Collaboration with regulatory, clinical, and safety teams is central to maintaining high-quality, audit-ready documentation.
This role involves leading scientific strategy and execution for immunogenicity and ligand binding assay (LBA) bioanalysis within Moderna’s mRNA-LNP therapeutic development programs. The Principal Scientist will oversee regulated assay development, validation, and sample testing, ensuring compliance with GcLP, GLP, and regulatory standards. The position emphasizes cross-functional collaboration, data interpretation, and integration of emerging technologies, including AI-enabled analytics, to support clinical decision-making across the drug development lifecycle.
This role involves designing and optimizing automated laboratory workflows for biomarker testing and sample management within Moderna’s Clinical Biomarker Laboratory. The engineer will lead integration of advanced liquid handling systems, develop data pipelines, and ensure compliance with regulatory standards, while collaborating across digital, operations, and vendor teams to build scalable, AI-enhanced automation platforms.
This role involves maintaining and improving CSL's global pharmacovigilance (PV) system, ensuring compliance with GVP and regulatory requirements. Responsibilities include leading investigations, managing deviations, coordinating inspections, and providing PV training across various functions and affiliates.
This role involves leading strategic sourcing and evaluation of late-stage external Hematology therapeutic area opportunities, from Phase 2 through marketed drugs. Responsibilities include engaging with Key Opinion Leaders, driving due diligence, and shaping the portfolio through high-impact partnerships.
Leads DMPK strategy to advance drug programs from discovery to clinical development, integrating predictive modeling and high-throughput data. Builds and guides a scientific team while collaborating across functions and external partners to de-risk and accelerate therapeutic pipelines with a tech-forward approach.
Leads and develops a team responsible for the delivery of clinical trial site management and monitoring within AstraZeneca’s UK Oncology portfolio. Oversees study execution from site selection to close-out, ensuring compliance with ICH-GCP and local regulations while driving quality, efficiency, and team performance. Works closely with cross-functional teams to align study planning, resource allocation, and operational delivery across clinical trials.
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...
Leads the development and execution of DMPK strategy across drug discovery and development programs, integrating predictive ADME modeling and high-throughput experimental data. Bridges computational and experimental teams to accelerate small molecule and emerging modality programs from hit identification through IND-enabling studies. Builds and mentors a high-performing DMPK team within a cross-functional, tech-driven drug discovery environment.
Mechanical Engineer - Programme Manager - Drug Delivery DevicesA period of significant growth has created an opportunity for a Programme Manager with a strong Mechanical Engineering background and deep, hands‑on experience in drug delivery device development. Based in Cambridge, you...
