Clinical Research Coordinator - Oncology Trial, Athens

About the role

iQVIA is looking for a Clinical Research Coordinator for a new part-time project in Athens, running for 6-7 months and supporting an oncology clinical trial on site. The role is up to 15-20 hours per week and acts as a key member of the site team, supporting investigators and ensuring the day-to-day delivery of the trial. It covers data entry, query resolution, patient recruitment and engagement.

Key responsibilities

• Support clinical research studies and maintain a safe study environment under the direction of the Principal Investigator
• Safeguard the well-being of study subjects and act as their advocate
• Maintain study protocols, case report forms, EDC systems and other study documents
• Plan and coordinate logistics for study procedures and perform clinical set-up, including labelling specimen tubes, managing supplies and setting up or troubleshooting equipment
• Assist with data entry, data quality checks and query resolution
• Help recruit, screen and orient volunteers, and assist in study enrollment
• Handle study drug custody according to site SOPs and coordinate with the study monitor

Required profile

• BS/BA in life sciences or educational equivalent, or relevant clinical research coordinator experience
• At least three years of experience in oncology clinical trials
• Knowledge of clinical trials, consent forms and study schedules
• Basic knowledge of medical terminology

Required skills

• MS Windows and Office applications such as Access, Outlook, Excel and Word
• Good organisational skills and attention to detail
• Strong interpersonal skills

The potential base pay range, when annualized, is EUR 27,400 to EUR 41,000, depending on qualifications, location and schedule; incentives and other benefits may also apply.