Clinical Trial Assistant - Sponsor Dedicated - Israel
On-siteNetanya, Central District, Israel
Job Summary
Maintain Trial Master Files and clinical documents by updating systems, tracking site compliance, and preparing reports according to standard operating procedures. Coordinate the distribution and archiving of clinical documentation, manage Case Report Forms and queries, and handle clinical trial supplies. Serve as the central contact for project communications and documentation while assisting Clinical Research Associates and Regulatory teams. May accompany CRAs on site visits to support clinical monitoring duties after completing required training. Requires 3-4 years of administrative support experience with a preference for one year in clinical research, including knowledge of Good Clinical Practice and ICH guidelines. Full-time hybrid role in Netanya, Israel. IQVIA accelerates the development of innovative medical treatments to improve patient outcomes worldwide.
Required Qualifications
- High School Diploma or equivalent
- 3-4 years administrative support experience
- Equivalent combination of education, training and experience
- Minimum one year clinical research experience
- Working knowledge of Microsoft Word
- Working knowledge of Excel
- Working knowledge of PowerPoint
- Good command of English language
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
- Basic knowledge of applicable clinical research regulatory requirement, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Knowledge of applicable protocol requirements
Desired Qualifications
- Minimum one year clinical research experience strongly preferred
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.