# Clinical Trial Assistant

**Company**: IQVIA
**Location**: Seoul, Republic of Korea
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Seoul-Republic-of-Korea/Clinical-Trials-Assistant--1-Year-Contract-_R1577873?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/clinical-trial-assistant-45d2e1bd-0df/

## Description

We are seeking a Clinical Trial Assistant to perform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams 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 (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.

- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.

- 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.

- Assist with the tracking and management of 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**

- Preferred: 1+ year of experience as a Clinical Trial Assistant (CTA) within a CRO or pharmaceutical company

- Preferred: Proficiency in both written and spoken English communication

- 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.

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

- Knowledge of applicable protocol requirements as provided in company training.

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## Skills

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

### Nice to have
- English

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Seoul-Republic-of-Korea/Clinical-Trials-Assistant--1-Year-Contract-_R1577873?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)