# Clinical Research Coordinator

**Company**: IQVIA
**Location**: Athens
**Work arrangement**: onsite
**Experience**: senior
**Job type**: part-time
**Salary**: €27,400.00 - €41,000.00
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Athens-Greece/Clinical-Research-Coordinator---Athens_R1577383?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_c5ad458f-1e1

## Description

We are seeking a Clinical Research Coordinator to join our team in Athens, Greece on a part-time basis for 15-20 hours per week. The role will last for 6-7 months and will support an oncology clinical trial on site.

As a key member of the site team, you will play an important role in supporting investigators and helping to ensure the smooth day-to-day delivery of clinical trials. You will act as the go-to person for data entry and query resolution, while also playing an active role in patient recruitment and engagement.

Responsibilities:

- Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator

- Safeguard the well-being of subjects, act as a volunteer advocate, and address subject's concerns

- Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents

- Plan and coordinate logistical activity for study procedures according to the study protocol

- Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues

- Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness

- Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol

- Correct custody of study drug according to site standard operating procedures

- Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.

Requirements:

- BS/BA in life sciences or educational equivalent and/or relevant work experience as a clinical research coordinator

- At least three years of experience in oncology clinical trials

- Excellent knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules

- Basic knowledge of medical terminology

- Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word

- Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client

- Good organizational skills with the ability to pay close attention to detail.

The potential base pay range for this role, when annualized, is €27,400.00 - €41,000.00.

## Skills

### Required
- clinical trials
- life sciences
- medical terminology
- MS Windows
- Office applications
- interpersonal skills
- organizational skills

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Source: [Apply at iqvia.wd1.myworkdayjobs.com](https://iqvia.wd1.myworkdayjobs.com/en-US/IQVIA/job/Athens-Greece/Clinical-Research-Coordinator---Athens_R1577383?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)