DescriptionJoin 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 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. 
