Clinical Trial Assistant 2 - Israel

About the role

IQVIA's Clinical Functional Service Partnership (CFSP) offers embedded members of pharmaceutical and biotechnology teams the variety of sponsor-level exposure and the stability of a global career. As a Clinical Trial Assistant 2 in Israel, you will gain hands-on exposure to real study operations, learn alongside experienced CRAs and Project Managers, and build a foundation for future clinical research roles.

Key responsibilities

• Maintain and update Trial Master Files (TMF) and study documentation
• Support document preparation, filing, tracking and archiving
• Review study files for completeness and compliance
• Coordinate clinical trial supplies and tracking records
• Assist with CRF tracking, study queries and data workflows
• Act as a key contact for project communications and documentation
• Guide and mentor Clinical Trial Assistants, supporting onboarding, training and knowledge sharing
• Serve as a subject matter expert for clinical trial processes, possibly leading CTA study teams and contributing to recruitment
• Support departmental quality and process improvement initiatives

Required profile

• Passion for clinical research and healthcare
• Science degree preferred
• Advanced Hebrew and English
• At least 1 year of clinical trials support experience
• Strong organisation skills, attention to detail and ability to manage multiple priorities and meet deadlines
• Effective communication and collaboration across teams

Required skills

• Proficiency in Microsoft Office (Word, Excel, PowerPoint)