# Clinical Research Administrative Assistant

**Company**: IQVIA
**Location**: Buenos Aires
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Buenos-Aires-Argentina/CTA_R1578484?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/clinical-research-administrative-assistant-fee35120-2ca/

## Description

We are seeking a highly organized and detail-oriented individual to join our team as a Clinical Research Administrative Assistant in Buenos Aires, Argentina.

As a Clinical Research Administrative Assistant, you will play a critical role in supporting the Clinical Research Associates and Regulatory and Start-Up teams to ensure the delivery of complete and accurate Trial Master Files.

Key responsibilities include:

- Assisting Clinical Research Associates and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems

- Preparing, handling, distributing, filing, and archiving clinical documentation and reports

- Reviewing study files for completeness

- Assisting with the preparation, handling, and distribution of Clinical Trial Supplies

- Tracking and managing Case Report Forms, queries, and clinical data flow

- Acting as a central contact for the clinical team for designated project communications and correspondence

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

Requirements:

- High School Diploma or equivalent

- 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 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

- Knowledge of applicable protocol requirements

At IQVIA, we create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

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## Skills

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

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Buenos-Aires-Argentina/CTA_R1578484?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)