# Clinical Research Administrative Assistant

**Company**: IQVIA
**Experience**: entry
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Beijing-China/CTA-KunTuo_R1554585?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_181ccc19-75a

## Description

Perform daily administrative activities to ensure a complete and accurate Trial Master File delivery.

Responsibilities:

- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with updating and maintaining clinical documents and systems.

- Prepare, handle, distribute, file, and archive clinical documentation and reports.

- Review study files for completeness.

- Assist with Clinical Trial Supplies and tracking information.

- Track and manage Case Report Forms (CRFs), queries, and clinical data flow.

- Act as a central contact for the clinical team for project communications.

- May accompany CRAs on site visits to assist with clinical monitoring duties.

Qualifications:

- High School Diploma or equivalent required.

- 3 years administrative support experience.

- Computer skills including Microsoft Word, Excel, and PowerPoint.

- Good command of English language.

- Effective time management and organizational skills.

- Ability to establish and maintain effective working relationships.

- Awareness of clinical research regulatory requirements (GCP and ICH guidelines).

## Skills

### Required
- Microsoft Word
- Excel
- PowerPoint
- Good Clinical Practice (GCP)
- International Conference on Harmonization (ICH) guidelines
- English

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