Future Tech Jobs
Future Tech Jobs
This role involves leading the clinical pharmacology and pharmacometrics strategy for rare disease and oncology programs, designing clinical studies, and authoring regulatory documents. You will work closely with cross-functional teams to solve drug development challenges and expedite decision-making through modeling and simulation.
This role involves executing high-throughput, multi-omics screening experiments using automated lab systems in 384- and 1536-well plates to generate data for drug discovery. The candidate will prioritize production workflows, maintain equipment and reagents, and contribute to process improvements through automation and optimization. Collaboration, proactive communication, and adherence to SOPs are essential in this fast-paced, mission-driven environment.
This role involves performing and managing GMP and compliance audits of Biopharm, Vaccines, and Pharmaceutical facilities. You will evaluate compliance with GMP, policies, and regulatory requirements, and provide subject matter expertise on sterile manufacturing. The role requires strong communication and influencing skills, and involves travel to various sites across the network.
This role involves performing and managing GMP and compliance audits of GSK's Biopharm, Vaccines, and Pharmaceutical facilities across the EMEA region. You will evaluate compliance with GMP, regulatory requirements, and quality management systems, and provide subject matter expertise in sterile manufacturing. The role requires strong communication and influencing skills to engage with senior stakeholders and produce clear audit reports.
This role involves applying physical organic chemistry and digital modelling to develop scalable, sustainable manufacturing processes for pharmaceuticals. The scientist will lead mechanistic understanding, design experiments, and integrate automation and data-driven approaches to optimise synthetic routes. Collaboration with analytical chemists, engineers, and data scientists is central to driving innovation in drug substance development.
This role leads sustainability strategy within AstraZeneca's Chemical Development department, embedding green chemistry principles across process development and commercialisation. The director will drive innovation in environmental sustainability, oversee compliance, and act as a key advisor to CDMO partners to reduce carbon footprint and resource consumption across the supply chain. Collaboration with cross-functional teams and external stakeholders is central to advancing the company’s long-term sustainability goals.
The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust data analysis and regulatory compliance. They collaborate with cross-functional teams, manage external partners, and represent Biostatistics in regulatory interactions.
The Director of Biostatistics leads the statistical aspects of clinical development programs, ensuring robust study design, data analysis, and regulatory submissions. They collaborate closely with cross-functional teams and regulatory authorities to drive the success of clinical trials and ensure high-quality statistical insights.
This role involves developing, optimizing, and validating ligand-binding and cell-based assays to support mRNA medicine development. The candidate will generate pharmacodynamic and immunogenicity data in compliance with GcLP, using platforms like Watson LIMS and electronic lab notebooks. They will also contribute to reagent management, assay documentation, and cross-functional collaboration with clinical teams to ensure robust, regulatory-compliant data delivery.
This role involves developing and implementing CMC regulatory strategies for international submissions, providing guidance on regulatory CMC aspects, and leading discussions with health authorities. The candidate will also support the creation of CMC submission templates and offer interpretations of regulatory guidance documents, ensuring compliance and efficient delivery of high-quality regulatory documentation.
This role involves leading translational medicine strategies in dermatology, spanning early to late-stage drug development. The expert will drive clinical pharmacology, biomarker development, and regulatory strategies while collaborating across research, development, and external stakeholders. Key responsibilities include study design, safety oversight, and scientific leadership in global project teams.
Salary Range:£78,400.00 - £145,600.00Job Description Summary#LI-HybridLocation: London (The Westworks), United KingdomRelocation Support: This role is based in London (The Westworks), United Kingdom. Novartis is unable to offer relocation support: please only apply if accessible.Shaping the future of clinical development requires...
In this role, you will develop and lead complex projects, manage economic research studies for clinical trials, and formulate research plans. You will also collaborate with sales teams to maximize sales and enhance customer interactions using health economic models.
This role involves providing strategic and operational expertise for the disclosure of clinical regulatory documents on public websites, ensuring compliance with global regulatory requirements. Responsibilities include managing disclosure activities, overseeing vendors, and developing standard processes and technologic solutions to support transparency in clinical trials.
Isomorphic Labs is applying frontier AI to help unlock deeper scientific insights, faster breakthroughs, and life-changing medicines with an ambition to solve all disease.The future is coming. A future enabled and enriched by the incredible power of machine learning. A...
