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.