17h ago
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Clinical Trials Assistant II

United KingdomUnited Kingdom·Readingmid
OtherAssistant
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Quick Summary

Key Responsibilities

This role is not eligible for UK visa sponsorship. Apply today and forge a career with greater purpose, make an impact, and never stop learning!

Technical Tools
OtherAssistant

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

~1 min read
  • →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
  • Passion for clinical research and healthcare
  • Science degree preferred
  • Previous administrative, coordination, or healthcare-related 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.

Location & Eligibility

Where is the job
Reading, United Kingdom
On-site at the office
Who can apply
Open to applicants worldwide

Listing Details

Posted
October 2, 2026
First seen
October 2, 2026
Last seen
October 2, 2026

Posting Health

Days active
0
Repost count
0
Trust Level
56%
Scored at
October 2, 2026

Signal breakdown

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Clinical Trials Assistant II