# Clinical Research Coordinator

**Company**: IQVIA
**Location**: Antwerp, Antwerp
**Work arrangement**: onsite
**Job type**: part-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Antwerp-Antwerp-Belgium/Clinical-Research-Coordinator---Turnhout_R1577435-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_d775ac01-ecd

## Description

IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Turnhout. This 8-10 hour per week role 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:

- Prescreening and Screening tasks

- Review charts from the site database

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

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

- Lab sample processing and shipment

- Use of IRT/IWRS systems for subject randomization, investigational product assignment, inventory management, and site-level clinical trial operations

- Patient scheduling support

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

- 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

- Experience with lab samples and IRT/IWRS systems

- Good knowledge of medical terminology

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

- At least 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 organizational skills and attention to detail

- Fluency in English

## Skills

### Required
- clinical trials
- study protocols
- consent forms
- medical terminology
- MS Office
- IRT/IWRS systems
- lab samples
- English

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Antwerp-Antwerp-Belgium/Clinical-Research-Coordinator---Turnhout_R1577435-1?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)