Quality Associate – Clinical Trials QA, On‑Site in London

St Pancras Clinical Research; Greater London; On-site; GBP 29,000 - 35,000; Full time

Job summary

St Pancras Clinical Research, a British award-winning Site Management Organisation, is seeking a Quality Associate for a full-time, on-site role at the London site with regular travel to other sites. You will support the implementation and maintenance of quality systems across clinical trial activities, ensuring SOP/GCP/regulatory compliance and contributing to data integrity and patient safety.

Qualifications include strong analytical skills, experience in quality control and audits, and a

Qualifications

• Strong analytical skills to interpret data 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

Responsibilities

• Monitor compliance with standard operating procedures (SOPs), Good Clinical Practice (GCP), and regulatory requirements.
• Conduct document reviews; assist with internal quality audits.
• Identify protocol deviations, support root-cause analysis, and implement corrective and preventive actions.
• Maintain quality documentation and contribute to training initiatives related to quality standards.
• Contribute to initiatives that enhance data integrity, patient safety, and sponsor confidence.

Skills

Quality systems

GCP & regulatory

Audits

Root cause analysis

Data integrity

Documentation review

Cross-functional teamwork

Attention to detail

Tools

Office software

Electronic Document Management System

Job description

St Pancras Clinical Research, a British award-winning Site Management Organisation, is seeking a Quality Associate for a full-time, on-site role at the London site with regular travel to other sites. You will support the implementation and maintenance of quality systems across clinical trial activities, ensuring SOP/GCP/regulatory compliance and contributing to data integrity and patient safety.

Qualifications include strong analytical skills, experience in quality control and audits, and a