# Clinical Research Administrative Assistant

**Company**: IQVIA
**Location**: Beijing, China
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Beijing-China/CTA2_R1543779?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_ef131c2e-71d

## Description

We are seeking a highly organized and detail-oriented Clinical Research Administrative Assistant to join our team in Beijing, China. As a Clinical Research Administrative Assistant, you will 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 accurately updating and maintaining clinical documents and systems.

- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports.

- Assist with periodic review of study files for completeness.

- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.

- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.

- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.

**Qualifications:**

- High School Diploma or equivalent required.

- 3-4 years administrative support experience.

- Minimum one year clinical research experience strongly preferred.

- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.

- Written and verbal communication skills including good command of English language.

- Effective time management and organizational skills.

- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

- Basic knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.

**Benefits:** No benefits information provided.

## Skills

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

### Nice to have
- clinical research experience

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Beijing-China/CTA2_R1543779?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)