Clinical Trials Coordinator II: TMF & Data Support

IQVIA; Reading; On-site; GBP 22,000 - 32,000; Full time

Job summary

IQVIA in Reading, Berkshire, United Kingdom is seeking a Clinical Trials Assistant (CTA I or CTA II) to support clinical studies by maintaining documentation, coordinating activities, and helping ensure projects stay compliant and on track. You will work closely with CRAs and Regulatory teams to gain insight into the clinical research process and contribute to healthcare innovation.

Key duties include TMF maintenance, document filing, review of study files for completeness, and coordinating

Qualifications

• Science degree preferred.
• Experience in administrative coordination or similar roles.
• Proficiency in Microsoft Office and data-tracking tools.
• Strong organisational and communication skills.

Responsibilities

• Maintain and update Trial Master Files (TMF) and study documentation.
• Support document preparation, filing, tracking, and archiving.
• Review study files for completeness and compliance.
• Coordinate clinical trial supplies and tracking records.
• Assist with CRF tracking, study queries, and data workflows.
• Act as a key contact for project communications and documentation.

Skills

Clinical research enthusiasm

Administrative coordination

Organizational skills

Communication skills

Education

Science degree preferred

Tools

Microsoft Office (Word, Excel, PowerPoint)

Job description

IQVIA in Reading, Berkshire, United Kingdom is seeking a Clinical Trials Assistant (CTA I or CTA II) to support clinical studies by maintaining documentation, coordinating activities, and helping ensure projects stay compliant and on track. You will work closely with CRAs and Regulatory teams to gain insight into the clinical research process and contribute to healthcare innovation.

Key duties include TMF maintenance, document filing, review of study files for completeness, and coordinating