Future Tech Jobs
Future Tech Jobs
For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to Cambridge. The location of this role will therefore subsequently change to Cambridge in...
For candidates seeking to be located at our Stevenage site, this role will temporarily be based at Stevenage. However, the Company plans to relocate its offices to Cambridge. The location of this role will therefore subsequently change to Cambridge in...
Salary Range:£96,036.50 - £178,353.50Job Description Summary#LI-HybridWork Arrangement: Hybrid WorkingLocation: London (The Westworks), United KingdomAre you passionate about shaping the future of clinical development and making a meaningful impact in Cardiovascular/Stroke medicine? We are looking for an experienced and visionary Senior...
This role leads clinical development for assigned assets in Internal Medicine within Pfizer's R&D division, serving as the primary clinical accountability point on the Global Medicine Team. The leader designs and executes global clinical development plans, guides cross-functional teams through trial phases, and supports regulatory submissions and lifecycle strategies. Emphasis is placed on innovation, patient engagement, and strategic external collaboration to advance obesity and internal medicine therapeutics.
This role involves leading clinical development for Internal Medicine assets within Pfizer's Research & Development division, with end-to-end accountability for creating and executing global clinical development plans. The position requires deep therapeutic expertise in chronic weight management or endocrinology, leadership of cross-functional teams, and active engagement in trial design, regulatory submissions, and lifecycle strategy. The role operates in a hybrid work model and may include responsibilities across the Obesity portfolio.
The Risk Surveillance Lead drives Risk-Based Quality Management (RBQM) adoption at the trial level, overseeing risk identification, mitigation, and continuous improvement across clinical trials. This role involves facilitating cross-functional risk assessments, managing quality tolerance limits, conducting central surveillance using RBQM analytics, and leading risk review discussions. It plays a key role in ensuring clinical quality governance and compliance with GCP standards within a matrix environment.
This role involves leading the development and validation of advanced molecular assays such as RT-qPCR, dPCR, and NGS to support clinical biomarker strategies across Moderna’s therapeutic pipeline. The scientist will work hands-on in assay design, optimization, and data interpretation, ensuring compliance with GCLP standards while integrating genomics, bioinformatics, and clinical insights. Collaboration with cross-functional teams is key to translating molecular data into actionable decisions for drug development.
This role involves leading the development and validation of advanced molecular assays (including RT-qPCR, dPCR, and NGS) to support clinical biomarker programs across Moderna’s therapeutic pipeline. The scientist will drive end-to-end assay lifecycle management, ensure regulatory compliance with GCLP standards, and collaborate with cross-functional teams to generate high-quality genomic data for clinical decision-making. Emphasis is placed on innovation, data integrity, and integrating emerging technologies like AI-enabled tools to accelerate translational research.
This role involves servicing and repairing advanced medical diagnostic and laboratory systems used in NHS and private healthcare settings. The engineer will conduct on-site maintenance, perform breakdown repairs, and provide technical troubleshooting support to laboratory staff. Full product training is provided, emphasizing customer service and technical reliability in a high-stakes clinical environment.
Install, maintain, and repair advanced medical diagnostic systems in NHS and private laboratory settings. Provide on-site technical support, troubleshoot complex instrumentation, and deliver high-quality customer service during service and breakdown calls. Work independently across a defined region with comprehensive training and support.
This role focuses on enabling secure and compliant cross-border data transfers for AstraZeneca’s Beijing AI Center, primarily from global R&D into China. The scientist will lead first-pass triage, provenance tracing, metadata coordination, and evidence preparation for data sharing requests, ensuring alignment with regulatory requirements like DOJ EO 14117 and internal governance. It bridges scientific data, compliance, and operational execution to accelerate AI-driven drug discovery while maintaining audit readiness and building scalable processes.
The Clinical Program Manager will lead the transition of internal drug programs from pre-IND stages into clinical trial execution, coordinating cross-functional global teams and external vendors. This role involves managing timelines, budgets, risks, and stakeholder communication, while leveraging AI-driven insights to accelerate development. The position emphasizes integrated project planning and operational leadership to ensure efficient, high-probability clinical advancement.
This role involves leading safety data review and pharmacovigilance activities within clinical trials, ensuring compliance with international regulations such as GxP. The individual will mentor team members, manage CAPAs, support regulatory inspections, and contribute to safety reporting and risk management. Key responsibilities include MedDRA coding, safety data analysis, and developing pharmacovigilance procedures to support global regulatory requirements.
This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while guiding cross-functional teams and managing vendor performance. They also support redaction of confidential information and drive process improvements across disclosure operations.
Lead clinical strategy and execution for early-phase trials, authoring key clinical documents and overseeing medical monitoring. Serve as primary liaison with investigative sites and internal teams, ensuring data integrity across multiple oncology and hematology studies. Operate in a fast-paced, AI-driven drug discovery environment with cross-functional collaboration.
