Clinical Trials Assistant II
IQVIA · Reading, UK
Clinical OperationsFull-timeCompany career page
RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.
Role summary
IQVIA seeks a Clinical Trials Assistant II to support clinical studies in Reading through documentation management, compliance oversight, and coordination of trial activities. The role involves working with clinical teams to maintain accurate records and ensure studies progress smoothly.
What they're looking for
- Science degree preferred
- Previous administrative, coordination, or healthcare-related experience
- Proficiency in Microsoft Office (Word, Excel, PowerPoint)
- Strong organisation skills and meticulous attention to detail
- Ability to manage multiple priorities and meet deadlines
- Effective communication and collaborative teamwork abilities
- Passion for clinical research and healthcare
What you'll be doing
- Maintain and update Trial Master Files and study documentation
- Support document preparation, filing, tracking, and archiving activities
- Review study files for completeness and regulatory compliance
- Coordinate clinical trial supplies and maintain tracking records
- Assist with Case Report Form tracking, study queries, and data workflows
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.