# 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/Taipei--Taipei-City-Taiwan/Clinical-Trials-Assistant--CTA-_R1532548?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_a8cba5ac-085

## Description

Perform daily administrative activities to ensure a complete and accurate Trial Master File delivery in conjunction with Clinical Research Associates and Regulatory and Start-Up teams.

**Essential Functions**

- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with updating and maintaining clinical documents and systems, such as Trial Master File (TMF), to track site compliance and performance within project timelines.

- Prepare, handle, distribute, file, and archive clinical documentation and reports according to the scope of work and standard operating procedures.

- Conduct periodic reviews of 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**

- High School Diploma or equivalent required.

- 3 years of administrative support experience.

- Equivalent combination of education, training, and experience.

- 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 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, as provided in company training.

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

## Skills

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

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