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Clinical Trial Assistant – Sponsor Dedicated (Netanya)

IQVIA · Netanya

New
🇬🇧 English
Microsoft Word

Job description

About the role

The Clinical Trial Assistant supports the Clinical Research Associates and Regulatory & Start‑Up teams in daily administrative activities, ensuring accurate trial documentation and compliance throughout the study lifecycle.

Key responsibilities

  • Assist CRAs and RSU team with updating and maintaining the Trial Master File and other clinical documents.
  • Prepare, handle, distribute, file and archive study documentation and reports according to SOPs.
  • Support the preparation, handling and distribution of clinical trial supplies and maintain tracking information.
  • Track and manage case report forms, queries and clinical data flow.
  • Act as a central contact for project communications and may accompany CRAs on site visits after training.

Required profile

  • High school diploma or equivalent.
  • At least three years of administrative support experience.
  • Strong written and verbal communication in English and Hebrew.
  • Effective time‑management and organizational abilities.
  • Awareness of GCP and ICH guidelines as provided in company training.

Required skills

  • Proficiency with Microsoft Word.
  • Proficiency with Microsoft Excel.
  • Proficiency with Microsoft PowerPoint.

Questions fréquentes

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Published 5 days ago

Expires 1 month from now

26 views · 0 interested

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IQVIA

Netanya