Leads global safety strategy for formulation safety within CSL's GSPV department, overseeing clinical safety evaluation across product lifecycles. Responsible for signal detection, risk management planning, and regulatory compliance across clinical development and post-marketing phases. Serves as safety representative in cross-functional teams, ensuring alignment with medical, regulatory, and business objectives.
This role involves servicing and repairing advanced medical diagnostic systems used in NHS laboratories and clinical chemistry environments. The engineer will visit customer sites to perform maintenance, troubleshoot issues, and deliver technical solutions while working closely with laboratory staff. The position requires a technically skilled individual with experience in high-value capital equipment and offers extensive product training.
Perform on-site installation, maintenance, and repair of advanced medical diagnostic systems in NHS and private laboratory settings. Provide technical troubleshooting and customer support across pathology and clinical chemistry environments. Receive full product training and work with cutting-edge diagnostic equipment from a global market leader.
The Feasibility Strategic Analytics Lead (FSAL) at Pfizer is responsible for providing robust assessments of clinical trial feasibility, recruitment, and site strategy. This role involves partnering with various teams to optimize country and site selection, leveraging data-driven insights, and driving continuous improvement in the clinical trial process.
The Feasibility Strategic Analytics Lead (FSAL) at Pfizer is responsible for providing robust assessments of program and protocol feasibility, driving country and site selection, and optimizing enrollment strategies. This role involves leveraging data-driven insights, benchmarking, and competitive intelligence to inform strategic decisions and enhance the efficiency of clinical trials.
This role leads global clinical trial disclosure and transparency strategy, ensuring compliance with international regulations such as FDAAA 801, EU CTR, and MHRA requirements. The individual oversees study registration, results reporting, and layperson summaries, while managing redaction of confidential information for public release. They act as a key liaison with regulatory bodies and internal teams, driving process efficiency and vendor performance across the clinical development lifecycle.
Lead the development and execution of translational medicine strategies for oncology programs, integrating AI-driven insights to inform clinical trial design and biomarker development. Collaborate with cross-functional teams to translate preclinical findings into clinical applications and advance companion diagnostics. Play a key role in shaping the scientific direction of early-stage drug development using cutting-edge methodologies and digital biology approaches.
The role involves end-to-end management of clinical trials within a fast-paced, AI-driven drug discovery environment. The Senior Clinical Trial Manager will lead cross-functional teams, oversee trial start-up through close-out, ensure compliance with ICH/GCP standards, and integrate AI innovations into clinical operations. Key responsibilities include vendor and budget management, clinical documentation, data oversight, and supporting regulatory readiness and audits.
This role involves ensuring the compliance, quality, and operational effectiveness of technology systems and facilities across engineering, logistics, and new product introduction at GSK’s Barnard Castle site. The specialist will support validation, maintenance, change control, and continuous improvement initiatives, providing quality oversight and driving audit readiness. The position offers broad exposure to smart manufacturing technologies and cross-functional collaboration in a regulated environment.
This role involves leading validation and computerised systems validation (CSV) activities for manufacturing processes, equipment, and systems within a GMP-regulated environment. You will support new product introductions, ensure compliance through risk-based documentation and quality oversight, and collaborate with engineering, IT, and manufacturing teams. The position plays a key part in maintaining regulatory standards and advancing smart manufacturing initiatives at GSK’s Barnard Castle site.
Lead the technical development and implementation of a new labeling and secondary packaging operation at Moderna's Harwell site, ensuring compliance with GxP and safety standards. Establish maintenance strategies, lead capital projects, and drive continuous improvement using engineering excellence principles. Work closely with global teams and support digital integration in a high-growth biotech environment.
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.
Leads global clinical strategy for Roche’s toxicology and drug testing portfolio, designing and executing clinical development programs to support regulatory approval and market adoption. Acts as scientific authority in interactions with health agencies, drives real-world evidence integration, and collaborates with KOLs and cross-functional teams to advance diagnostic innovation. Focuses on generating robust clinical evidence to demonstrate safety, effectiveness, and scientific validity of diagnostic solutions.
This role involves leading global clinical strategy for Roche’s toxicology and drug testing portfolio, including advanced diagnostic platforms like the cobas i601. The Clinical Development Lead will design and execute high-impact clinical programs, engage with regulatory authorities, integrate real-world evidence, and collaborate with key opinion leaders to drive diagnostic innovation and ensure scientific validity across global markets.
This role involves leading health, safety, and biological compliance across a gene therapy organisation, with a focus on regulatory adherence, risk assessment, and biosafety oversight. The specialist acts as the appointed Biological Safety Officer, ensuring safe handling of biological materials and driving a strong safety culture through training and audits. Work includes developing safety systems, incident investigation, and maintaining compliance with UK legislation and internal standards.
