Lead and execute model-informed drug development strategies in oncology, applying advanced pharmacometric and AI/ML techniques to optimize clinical trial design, dose selection, and regulatory submissions. Drive innovation in exposure-response analysis, population PK/PD, and quantitative systems pharmacology within a cross-functional R&D environment.
This role involves leading safety evaluation and risk management for GSK’s global pharmaceutical products, both in clinical development and post-marketing settings. The Safety Scientist will conduct signal detection, contribute to Risk Management Plans, author safety reports, and collaborate across functions to ensure patient safety. The position requires scientific rigor, regulatory knowledge, and strong cross-functional leadership in a hybrid working environment.
Leads the development and execution of precision medicine strategies within global clinical programs, focusing on biomarker and diagnostic initiatives to support patient selection and regulatory submissions in neuroscience. Acts as a scientific expert, leading cross-functional teams and ensuring compliance with medical device regulations. Facilitates collaborations with external research partners and drives operational excellence in biomarker strategy implementation.
Leads statistical programming for clinical studies across phases I-IV, ensuring high-quality, regulatory-compliant deliverables for regulatory submissions and clinical study reports. Develops and validates datasets and outputs using SAS, drives CDISC standards (SDTM/ADaM), and collaborates with biostatistics and cross-functional teams. Provides technical leadership, mentors junior programmers, and contributes to process improvements and programming specifications.
Lead regional regulatory strategy for oncology products across the Rest of World (ROW) region, aligning with global teams to ensure timely submissions, approvals, and commercially favorable labeling. Partner with project teams and health authorities to shape regulatory positions and influence the regional environment. Ensure compliance and effective implementation of regulatory standards throughout the product lifecycle.
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.
Lead and develop GMP/GDP audit strategy for a key technology area such as sterile biologics or medical devices, ensuring compliance with global regulations and emerging trends. Conduct complex audits across Pfizer facilities, contract manufacturers, and suppliers, while coaching auditors and driving continuous improvement in quality systems. Collaborate with cross-functional teams to assess risks, resolve findings, and prepare for regulatory inspections.
This role involves installing, maintaining, and repairing laboratory instruments—primarily water purification systems—in regulated environments across healthcare, life sciences, and electronics sectors. The engineer will conduct on-site visits throughout North/West London, performing troubleshooting, calibration, and customer training. A key aspect includes identifying and generating leads for new equipment and service contracts while ensuring high reliability of scientific instrumentation.
This role involves leading complex experimental workstreams in medical device R&D, from concept to design transfer, with a focus on diagnostic immunoassay technologies. The scientist will analyse multi-factorial data, optimise formulations using Design for Manufacture principles, and ensure compliance with GLP, GMP, and GDP standards in a laboratory setting. The position is based in Motherwell and supports critical development within a leading biopharmaceutical organisation.
We are partnering with a leading organisation in the Pharmaceutical, Healthcare and Retail Eye Care market, to recruit an impactful Pharmaceutical/Healthcare Sustainability Lead who will shape and drive the company’s environmental strategy. In this role, you’ll work closely with senior...
This role involves deploying and integrating generative AI models into pharmaceutical and biotech customers' scientific workflows. The engineer will lead end-to-end technical deployments, build production-grade API integrations and data pipelines, and act as a technical liaison between customers and internal research teams. A strong background in ML infrastructure, cloud platforms, and customer-facing delivery in life sciences is essential.
Evolve are partnering with a driven medical device manufacturer who are seeking a Connectivity Specialist to help shape the future of connected healthcare. This is an exciting opportunity to combine technical expertise, customer engagement, and project leadership to deliver innovative...
Lead the development of an AI scientist platform for drug discovery, combining multimodal biological data and agentic AI to automate target identification and hypothesis generation. Guide a team of data and research scientists in building systems that reason over omics, clinical, and literature data to accelerate pharmaceutical R&D. Work at the intersection of machine learning, computational biology, and pharmaceutical strategy.
Operate and maintain equipment in a cGMP-compliant, highly automated mRNA vaccine production environment at Moderna's Oxford facility. Perform production operations, support quality assurance, troubleshoot issues, and contribute to continuous improvement initiatives using digital systems and advanced manufacturing technologies. Work within a 2-2-3 rotating shift pattern to ensure reliable, safe, and compliant vaccine manufacturing.
Operate within a GMP-regulated warehouse environment at Moderna’s Harwell site, managing inbound and outbound material flows, inventory control via SAP, and supporting continuous mRNA manufacturing operations. Perform cycle counts, documentation, and logistics coordination while adhering to strict quality and safety standards. Gain exposure to digital-first and AI-enabled tools within a fast-paced, collaborative pharmaceutical setting.
