# CTA-KunTuo

Hiring organization: [IQVIA](https://career.thegoodapps.co/organizations/iqvia)

Canonical page: https://career.thegoodapps.co/jobs/c2bcb805-b63c-4740-9cc4-4922853f6e43

Listed on IQVIA's own careers site. Applications go to them directly.


## Summary

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._

## Skills named

Microsoft Excel, Microsoft PowerPoint, Microsoft Word

## 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

Apply on IQVIA's site: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Beijing-China/CTA-KunTuo_R1554585
