This role involves leading epidemiology programs, designing and delivering observational studies using real-world data, and collaborating with cross-functional teams. The position offers opportunities for growth and impact in the development and lifecycle of pharmaceutical products.
This role involves leading the clinical development of oncology drugs, specifically in genitourinary cancers. Responsibilities include defining clinical strategies, leading governance discussions, and representing the asset in external engagements. The role emphasizes data-driven decision-making and leveraging advanced analytics to enhance development speed and precision.
This role involves performing high-quality analytical chemistry and stability testing, supporting manufacturing processes, and maintaining GMP compliance. You will work with advanced analytical technologies and laboratory information systems to ensure the quality and integrity of mRNA materials and products.
This role involves performing routine cGMP Quality Control testing, including analytical chemistry and stability testing, to ensure the quality and integrity of materials and products. You will work with advanced analytical technologies and laboratory information systems to support manufacturing, product release, and regulatory compliance.
Lead the development and execution of nonclinical safety strategies for small molecule drug candidates in oncology and non-oncology programs, integrating AI-driven predictive models with traditional toxicology. Build and scale the nonclinical safety function within an AI-first drug discovery environment, ensuring high-quality data feedback to refine computational models. Collaborate across preclinical, clinical, and regulatory teams to advance compounds through IND and NDA/MAA-enabling studies.
This is a general interest application for roles at Isomorphic Labs, an AI-driven drug discovery company. Candidates may be considered for positions including Software Engineers, ML Researchers, Computational Chemists, and Technical Project Managers. The role involves interdisciplinary collaboration to advance AI models for rational drug design and digital biology, within a culture emphasising curiosity, bravery, determination, and teamwork.
This is a general talent network sign-up opportunity rather than a specific job role. Candidates can submit their resume for future consideration at Recursion, a clinical-stage TechBio company using AI and automated biology to accelerate drug discovery. The company emphasizes bold, ethical innovation and cross-functional collaboration to address unmet medical needs.
The Central Monitor (CM) is responsible for overseeing clinical trials through centralized monitoring, ensuring data quality, identifying risks, and enhancing trial oversight. They collaborate with cross-functional teams, configure monitoring technology, and communicate findings to stakeholders.
The Central Monitor (CM) is responsible for overseeing clinical trials through centralized monitoring, ensuring data quality, identifying risks, and collaborating with cross-functional teams. Key responsibilities include executing monitoring strategies, conducting data surveillance, and supporting risk management processes.
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 using advanced immunological techniques and serve as a subject matter expert within cross-functional teams. Emphasis is placed on innovation, scientific rigor, and integration of emerging technologies including digital and AI-enabled workflows in a GCP/GLP-regulated environment.
Operate production equipment for mRNA vaccine manufacturing in compliance with cGMP and safety standards. Perform routine maintenance, support deviation investigations, and contribute to continuous improvement in a highly regulated, technology-driven environment. Work collaboratively with QA and cross-functional teams to ensure timely batch disposition and operational excellence.
This role involves developing and executing biochemical and molecular biology assays to support pharmacokinetic/pharmacodynamic analysis. Responsibilities include assay development, data analysis, and collaboration with external partners, while staying current with scientific literature and regulatory guidelines.
This role involves leading the creation and management of investigator site budgets and contracts for clinical trials, using Grants Manager and FMV benchmarking tools. The candidate will oversee CRO activities, ensure budget consistency across trials, and support timely site activation by managing negotiations and identifying risks. Collaboration with legal, clinical operations, and external partners is central to ensuring compliance and efficiency in contract execution.
