Clinical Trials Assistant I

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

Reading, Berkshire, United Kingdom

Full time

R1571552

Join IQVIA on our mission to accelerate innovation for a healthier world!

As a Clinical Trials Assistant (CTA I OR CTA II), you'll support clinical studies by maintaining accurate documentation, coordinating study activities, and helping ensure projects stay compliant and on track. Working closely with Clinical Research Associates (CRAs) and Regulatory teams, you'll gain valuable exposure to the clinical research process while contributing to meaningful healthcare innovation.

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

What You'll Bring

• Passion for clinical research and healthcare
• 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)
• Strong organisation skills and attention to detail
• Ability to manage multiple priorities and meet deadlines
• Effective communication skills with the ability to work collaboratively across teams

Please note: This role is not eligible for UK visa sponsorship.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.

To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

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