IQVIA

Clinical Research Coordinator - Athens

Athens, Greece
Full-time
Posted Oct 30, 2026

Skills

Data Entry
Microsoft Excel
Recruiting
Troubleshooting

Job description

Are you looking for an opportunity in Clinical Research? Do you want to work for an industry leading company. If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.

We have a new part time project in Athens for up to 15-20 hours per week . It will be for 6-7 months and will support an oncology clinical trial on site in Athens.

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 . This is a varied position offering the opportunity to make a meaningful contribution to the successful delivery of clinical research.

Day to day responsibilities will include:

•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.

We are looking for candidates with the following skills and experience:

•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.

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is €27,400.00 - €41,000.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.