Clinical Research Coordinator
4 weken geleden
We are seeking a highly skilled and detail-oriented Site Research Assistant to join our team at IQVIA. As a pivotal member of our site team, you will play a crucial role in supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies.
Key Responsibilities:- 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
- 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
- BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting
- Good 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 clients
- Good organizational skills with the ability to pay close attention to detail
- Fluent Dutch with good English language skills
If you are a motivated and detail-oriented individual with a passion for clinical research, we encourage you to apply for this exciting opportunity to join our team at IQVIA.
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