Future Tech Jobs
Future Tech Jobs
Manages clinical trial operations from start-up to closure, coordinating with CROs and internal teams to ensure timely delivery of trials in oncology and rare diseases. Focuses on process improvements and operational excellence within a fast-paced, AI-driven drug discovery environment.
The Senior Clinical Project Manager will lead the execution of one or more clinical trials from start to finish, ensuring compliance with regulations and managing cross-functional teams. This role involves planning, budgeting, and overseeing global clinical trials, with a focus on early phase oncology studies.
As a Data Curator at Isomorphic Labs, you will work closely with AI experts and drug discovery scientists to curate high-quality, ML-ready datasets. Your role involves integrating large-scale biomedical and biochemical data, enhancing data quality, and collaborating across teams to build and improve data assets that fuel the company's mission to accelerate drug discovery using AI.
As a Data Scientist at Isomorphic Labs, you will work with a multidisciplinary team to analyze business intelligence data, implement telemetry, and design key metrics to optimize the drug design process. Your role involves providing actionable insights to drive decision-making across product, engineering, and research teams, and collaborating to build an analytics layer that supports efficient drug discovery.
The Onyx Research Data Tech organization represents a major investment by GSK R&D and Digital & Tech, designed to deliver a step-change in our ability to leverage data, knowledge, and prediction to find new medicines. We are a full-stack shop...
This role leads the planning and execution of translational medicine strategies for GSK's antibody-drug conjugate (ADC) oncology portfolio. The Director drives cross-functional coordination across biomarkers, diagnostics, and clinical development, ensuring integrated project plans, governance readiness, and operational excellence. They provide strategic project management leadership, risk oversight, and insight-driven reporting to support R&D decision-making across the global oncology pipeline.
This role leads the negotiation and execution of clinical trial contracts with investigator sites globally, managing both contractual terms and site budgets. The Senior Manager oversees complex or high-priority studies, resolves escalations, and collaborates with Legal, Finance, and pCRO partners to ensure timely site activation. It involves shaping contracting strategies, mentoring junior staff, and driving process improvements in a remote, global environment.
This role involves leading label design, production, and system operations for clinical trial supplies within a GMP and regulatory-compliant environment. The Senior Manager ensures accurate and timely delivery of packaging and labeling solutions using enterprise systems like PRISYM360 and EMD365, while driving process improvements and digital innovation. Collaboration with internal teams and external vendors is key to supporting global clinical studies and advancing supply chain traceability and efficiency.
This role involves leading an analytical team in early chemical development, ensuring the delivery of high-quality analytical work to support GMP manufacturing and stability. The position requires extensive experience in analytical science, a passion for team development, and the ability to drive organizational effectiveness and innovation.
This role involves leading and influencing strategic decisions in AstraZeneca's Oncology Global Programme Management, focusing on TDR, DDR, and Epigenetics. You will guide comprehensive programme strategies, connect various stages of drug development, and ensure optimal portfolio delivery.
The Associate Director, Biostatistics, leads the statistical contribution to clinical development programs, defining statistical strategies, ensuring appropriate methodologies, and collaborating with cross-functional teams. They also manage outsourcing operations, represent Biostatistics in regulatory interactions, and support innovation in clinical trial design and analysis.
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 Senior Principal Statistical Programmer leads statistical programming activities for multiple clinical studies or large projects, ensuring high-quality and timely deliverables. They collaborate with biostatistics, coordinate programming teams, and maintain compliance with industry standards.
The Global Asset Study Manager (GASM) at Roche/Genentech is responsible for the efficient execution of global clinical trials, ensuring consistency and compliance with IHC-GCP and Roche processes. Key responsibilities include coordinating study management, developing essential documents, driving innovation, and maintaining inspection readiness.
This role involves developing, optimizing, and validating molecular bioanalytical assays—such as qPCR, ddPCR, and RNA isolation—to support clinical-stage mRNA programs in a GCL0-compliant environment. The scientist will generate high-quality PK/PD data, ensure regulatory compliance, and collaborate across functions to advance assays from research into clinical development. Emphasis is placed on data integrity, digital innovation, and integration of emerging technologies including automation and AI-enabled workflows.
