Clinical Trials Assistant I: Launch Your Research Career

IQVIA; Reading; On-site; GBP 24,000 - 30,000; Full time

Job summary

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

This full-time role requires strong organization, attention to detail, and excellent

Qualifications

• Science degree preferred.
• Previous administrative, coordination, or healthcare-related experience or equivalent combination of education, training and experience.
• Proficiency in Microsoft Office (Word, Excel, PowerPoint).

Responsibilities

• Maintain and update 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

Organization

Attention to detail

Multitasking

Communication

Collaboration

Healthcare interest

Education

Science degree preferred

Tools

Microsoft Office

Job description

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

This full-time role requires strong organization, attention to detail, and excellent