Future Tech Jobs
Future Tech Jobs
This role involves leading clinical development strategies for aging-related research within GSK’s Respiratory, Immunology & Inflammation unit. The Medical Director will design and deliver translational and clinical plans, oversee study execution, and provide scientific leadership across cross-functional teams. The position emphasizes innovation in immune science and data-driven decision-making to advance novel medicines through the pipeline.
Leads clinical development for respiratory programs within GSK’s R&D pipeline, driving translational and clinical strategies from early to late stages. Provides medical oversight, designs studies, and collaborates across functions to deliver innovative medicines addressing immune-mediated respiratory diseases. Engages with regulators, investigators, and internal teams to advance asset development and shape future treatment paradigms.
Leads clinical development for assigned assets in Internal Medicine, driving global clinical strategy, trial design, execution, and regulatory submissions. Serves as primary clinical accountability, collaborating with cross-functional teams and external stakeholders to advance drug development programs from concept through approval, with potential focus on obesity-related therapeutics.
This role leads clinical development for Internal Medicine assets within Pfizer's Research & Development division, with accountability for designing and executing global clinical development plans. The position involves leading cross-functional teams, driving regulatory submissions, and serving as a therapeutic expert in obesity and related areas. It requires collaboration with internal and external stakeholders, including regulatory authorities and advisory boards, to shape clinical strategy and ensure successful drug development.
The role involves transforming complex clinical trial data into actionable insights to improve decision-making across clinical teams. You will collaborate with data quality and monitoring teams to enhance data strategy, implement risk-based analytics, and drive operational improvements using tools like Power BI and Spotfire. The position emphasizes data storytelling, advanced analytics, and leveraging technology transformation to support clinical trial oversight and patient outcomes.
This role involves providing clinical leadership in neuroscience drug development, with a focus on neuromuscular or related neurological disorders. The Medical Director will shape global clinical strategy, lead trial execution, and guide regulatory submissions while collaborating with cross-functional teams and external experts. It emphasizes scientific innovation, particularly in gene therapy, within a dynamic, international environment.
This role involves servicing and repairing advanced medical diagnostic systems used in NHS and private laboratories. The engineer will conduct on-site maintenance, troubleshoot technical issues, and deliver customer support for complex laboratory analysers. Full product training is provided, with a focus on pathology and clinical chemistry equipment.
This role involves installing, maintaining, and repairing advanced medical diagnostic systems used in NHS and private pathology laboratories. The engineer will provide on-site technical support, troubleshoot complex issues, and ensure equipment operates reliably. Full product training is provided, and the role offers extensive customer interaction across healthcare and scientific environments.
This role involves managing end-to-end clinical supply operations for Moderna’s mRNA-based therapies, ensuring investigational products are labeled, packaged, and distributed efficiently and in compliance with regulatory standards. The specialist coordinates with CROs, vendors, and internal teams to maintain supply chain continuity, troubleshoot logistics, and support digital innovation in supply systems, including AI-enabled tools and IRT platforms.
This role involves leading the development, qualification, and execution of complex cell-based immunoassays to support Moderna’s clinical trials across multiple therapeutic areas. The scientist will generate high-quality, regulatory-compliant data, serve as a subject matter expert, and collaborate with cross-functional teams and external partners. Emphasis is placed on assay innovation, scientific rigor, and integration of emerging technologies including digital and AI-enabled workflows.
This role involves performing analytical testing and processing of patient samples in a clinical laboratory, ensuring accurate and timely results. The scientist will validate tests, maintain equipment, and comply with quality standards like ISO 15189 and UKAS. Close collaboration with healthcare teams supports patient care within a regulated environment.
This role involves managing regulatory submissions and product lifecycle compliance for pharmaceutical products, with a focus on packaging, labelling, and interactions with the MHRA. The candidate will coordinate eCTD submissions, support variations, and ensure change control processes are followed across cross-functional teams. It's a hands-on position offering impact in a regulated environment with hybrid working and a clear regulatory focus.
Lead hospital account strategy across Devon and Cornwall to drive adoption of respiratory therapies within the NHS. Develop omnichannel engagement plans, leverage NHS data to identify opportunities, and collaborate with medical and market access teams to improve patient pathways and deliver commercial results. The role focuses on building relationships with healthcare professionals and decision-makers in secondary care and primary care networks.
Lead the development and execution of hospital account strategies across Devon and Cornwall to drive adoption of respiratory therapies within the NHS. Use omnichannel engagement, real-world NHS data, and cross-functional collaboration to influence patient pathways and deliver measurable commercial and health outcomes. Focus on building credibility with healthcare professionals and key decision-makers in secondary care and primary care networks.
Located within CSLB’s GSPV department, the Director, Global Safety Lead, Formulation Safety provide expertise on all aspects of –clinical safety throughout the entire lifecycle of a product with special emphasis on ongoing evaluation of safety information during clinical development and...
