# Clinical Research Administrative Assistant

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

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Prague-Czech-Republic/CTA-1---One-Sponsor-dedicated--Prague_R1578170?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_3c0e1b00-9d9

## Description

We are seeking a highly organized and detail-oriented individual to join our team as a Clinical Research Administrative Assistant in Prague, Czech Republic. You will play a critical role in supporting the Clinical Research Associates and Regulatory and Start-Up teams to ensure accurate and timely delivery of clinical trial documents.

**Responsibilities**

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

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

- Serve 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

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

- Excellent written and verbal communication skills, including a good command of the 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, such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

**What We Offer**

- Competitive salary

- Opportunity to work with a leading global provider of clinical research services

- Collaborative and dynamic work environment

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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/Prague-Czech-Republic/CTA-1---One-Sponsor-dedicated--Prague_R1578170?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)