# Travel Site Research Assistant / Clinical Research Coordinator – Czech Republic (Part-Time, 2 Days per Week)

**Company**: IQVIA
**Location**: Plzeň
**Work arrangement**: hybrid
**Experience**: mid
**Job type**: part-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/PlzePilsen-Czech-Republic/Travel-Site-Research-Assistant---Clinical-Research-Coordinator---Czech-Republic--2-days-per-week--_R1577971?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_225f76a7-b4f

## Description

IQVIA is currently recruiting a dedicated Site Research Assistant / Clinical Research Coordinator to support a clinical research site in Mariánské Lázně.

The opportunity is open to candidates from across the Czech Republic who are willing to travel to the site. The position is planned for 2 on-site days per week, which may be arranged as consecutive days. An overnight stay may also be considered if required.

### Key Responsibilities

As a key member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical research support tasks, including:

- Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems

- Supporting patient screening and enrollment, including handling informed consent and privacy documentation

- Coordinating logistical activities for study procedures in line with the study protocol

- Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness

- Managing and shipping biological samples

- Communicating with study monitors and responding to study-related inquiries

- Carrying out general administrative tasks related to the study

### Your Profile

- Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting

- At least 1–2 years of experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site

- Solid understanding of clinical trials and familiarity with study protocols, informed consent forms and study schedules

- Good knowledge of medical terminology

- Strong IT skills, including proficiency in MS Office applications

- Excellent interpersonal and communication skills

- Strong organizational skills and attention to detail

- Fluency in Czech and a good command of English

- Willingness to travel to Mariánské Lázně for 2 on-site days per week

### The Opportunity

This is a part-time assignment for approximately 6 months, offering the opportunity to work directly with a clinical research site and contribute to the successful delivery of a clinical trial.

Candidates from across the Czech Republic who are open to a travel-based setup are encouraged to apply.

## Skills

### Required
- Clinical Research
- Life Sciences
- Medical Terminology
- MS Office
- Czech
- English

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/PlzePilsen-Czech-Republic/Travel-Site-Research-Assistant---Clinical-Research-Coordinator---Czech-Republic--2-days-per-week--_R1577971?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)