CTA-KunTuo
IQVIAListed on IQVIA’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
This role supports clinical research teams by managing Trial Master Files, clinical documentation, and case report forms to maintain compliance and data integrity throughout study timelines. It suits detail-oriented administrative professionals with clinical research interest who can organize complex documentation and work effectively across multiple teams.
Our summary, not IQVIA’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- High school diploma or equivalent
- 3 years administrative support experience
- Computer skills in Microsoft Office applications
- Written and verbal communication skills with good English command
- Effective time management and organizational skills
- Ability to work effectively with coworkers, managers, and clients
- Awareness of Good Clinical Practice (GCP) and ICH guidelines as provided in training
- Knowledge of applicable protocol requirements as provided in training
Nice to have
- Equivalent combination of education, training and experience