# Clinical Research Assistant

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

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Chengdu-Sichuan-China/CTA_R1531096?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_c54502da-e5b

## Description

We are seeking a Clinical Research Assistant to support our clinical research team. As a Clinical Research Assistant, you will play a crucial role in ensuring the smooth operation of clinical trials.

Responsibilities:

- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems, such as Trial Master File (TMF)

- Prepare, handle, distribute, file, and archive clinical documentation and reports according to standard operating procedures

- Review study files for completeness

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

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

- 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:

- Bachelor's degree and above

- 1-3 years of administrative support experience

- Equivalent combination of education, training, and experience

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

- Excellent written and verbal communication skills, including good command of English language

- Effective time management and organisational skills

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

- Awareness of applicable clinical research regulatory requirements, such as Good Clinical Practice (GCP) and International Conference on Harmonisation (ICH) guidelines

- Knowledge of applicable protocol requirements

## Skills

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

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Chengdu-Sichuan-China/CTA_R1531096?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)