Role Description The Quality Associate is a full-time, on-site role based at the London site (travel required to other sites regularly). This role supports the implementation and maintenance of quality systems across clinical trial activities and site operations. Day-to-day tasks include monitoring compliance with standard operating procedures (SOPs), Good Clinical Practice (GCP), and regulatory requirements; conducting document reviews; and assisting with internal quality audits. The Quality Associate collaborates with clinical and operations teams to identify protocol deviations, support root-cause analysis, and implement corrective and preventive actions, as well as conducting internal audits on a day to day basis.. Additional responsibilities include maintaining quality documentation, supporting training initiatives related to quality standards, and contributing to initiatives that enhance data integrity, patient safety, and sponsor confidence.

• QualificationsStrong analytical skills to interpret data, identify trends, and support root-cause analysis
• Experience in quality control activities, such as reviewing documentation, verifying data accuracy, and monitoring adherence to procedures
• Knowledge of quality assurance principles, including oversight of processes, risk management, and compliance with GCP and regulatory standards
• Supporting quality auditing practices, including conducting regular internal audits and preparing for inspections
• Understanding of quality management frameworks and systems within clinical research
• Extensive previous experience in quality sector of clinical research is required
• Excellent attention to detail, organisational skills, and the ability to manage multiple tasks and deadlines
• Effective written and verbal communication skills, with the ability to work collaboratively in cross-functional teams
• Proficiency with standard office software and electronic document management systems
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