# Site Research Assistant / Clinical Research Coordinator

**Company**: IQVIA
**Location**: Mariánské Lázně
**Work arrangement**: onsite
**Experience**: mid
**Job type**: part-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/PlzePilsen-Czech-Republic/Clinical-Research-Coordinator---Marinsk-Lzn_R1574257-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_1c84ef59-02a

## Description

IQVIA is currently recruiting a dedicated Site Research Assistant /Clinical Research Coordinator to support a clinical research site in Mariánské Lázně. This part-time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.

**Key Responsibilities** As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical 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** We are looking for candidates who bring a combination of education, experience, and skills:

- Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)

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

- Good knowledge of medical terminology

- Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)

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

- Excellent interpersonal and communication skills

- Strong organisational skills and attention to detail

- Fluency in Czech and good command of English

**Why Join IQVIA?** At IQVIA, you will be part of a global team that is advancing healthcare through data, technology, and human science. We offer a supportive work environment, impactful projects, and the opportunity to make a real difference.

## Skills

### Required
- clinical trials
- study protocols
- medical terminology
- MS Office
- Czech
- English

---

Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/PlzePilsen-Czech-Republic/Clinical-Research-Coordinator---Marinsk-Lzn_R1574257-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)