Future Tech Jobs
Future Tech Jobs
This role involves leading the clinical development of a medicine, managing a cross-functional team, and ensuring high-quality clinical and scientific standards. Responsibilities include strategic leadership, clinical oversight, and authoring key study documents and regulatory submissions.
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 working on a leading-edge automation platform to develop and run biochemical and cell-based assays, ensuring high-quality data for drug discovery projects. You will collaborate with cross-functional teams, innovate in laboratory automation, and contribute to the rapid identification of candidate molecules.
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 ensuring compliance with quality standards in a fast-paced, cutting-edge biopharmaceutical environment.
Nuclera is a venture-backed, founder-driven biotech company headquartered in Cambridge, UK with significant operations in Boston, USA. The company’s mission is to improve human health by making proteins accessible. We are beginning this mission through the launch of our eProtein...
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 analyzing the impact of environmental aerosol exposures on immune cells using advanced sequencing techniques and metabolomics. The successful candidate will work on a project led by Prof Nnenna Kanu, focusing on how these exposures affect immune and epithelial cells in mouse models and comparing the findings to human data.
This role involves providing hands-on IT support for Moderna’s GMP manufacturing operations at the Harwell site. Key responsibilities include ensuring GMP compliance, triaging IT incidents, managing infrastructure, and collaborating with various teams to maintain robust and compliant systems. The position offers exposure to modern observability and cybersecurity tools, making it a dynamic opportunity for someone who thrives in complex, regulated environments.
This role involves supporting Moderna’s manufacturing operations at the Harwell site, ensuring GMP compliance and providing Tier 1 IT support. Responsibilities include maintaining robust IT systems, triaging incidents, managing infrastructure, and collaborating with various teams to ensure smooth operations. The position offers exposure to modern cybersecurity and automation tools, making it a dynamic and challenging opportunity in the biotech industry.
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 supporting the delivery of clinical studies from protocol development to final reporting. Responsibilities include maintaining the Trial Master File, coordinating cross-functional teams, and ensuring regulatory compliance. The position is ideal for someone early in their clinical research career who enjoys organization and collaboration.
The role involves leading the sourcing, acquisition, and stewardship of human samples and translational data to support GSK's discovery and development efforts. Key responsibilities include strategic planning, stakeholder management, sample and data acquisition, re-use of internal samples, building external partnerships, and ensuring compliance with ethical and regulatory standards.
This role involves conducting advanced in vitro and ex vivo research to identify and validate therapeutic targets for obesity. The successful candidate will work in a dynamic, collaborative environment, designing and implementing experiments, analyzing data, and contributing to drug discovery projects across multiple sites.
This role involves providing medical and scientific expertise in the safety evaluation and risk management of 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.
This role involves providing statistical support for clinical trial design and analysis, focusing on biomarker discovery and validation. The position requires developing innovative study designs, crafting adaptive trial protocols, and collaborating with cross-functional teams to implement statistical analysis plans and interpret results.
