Clinical Files Specialist – Entry Level
iqvia · Buenos Aires
Job description
About the role
This entry-level position supports Clinical Research Associates and the Regulatory & Start‑Up team in maintaining accurate trial documentation. The role is hybrid, requiring occasional office attendance.
Key responsibilities
- Update and maintain clinical documents and systems, including the Trial Master File, to track site compliance and performance.
- Assist with regulatory documentation, preparation, handling, distribution, filing and archiving of clinical reports.
- Support periodic review of study files for completeness and assist with clinical trial supplies tracking.
- Help manage Case Report Forms, queries and clinical data flow.
Required profile
- Bachelor’s degree in Life Sciences or Healthcare.
- 1–2 years of administrative support or internship experience in clinical research or pharma.
- Strong written and verbal English communication skills.
- Effective time‑management, organizational abilities and teamwork orientation.
Required skills
- Proficiency with Microsoft Word, Excel and PowerPoint.
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Published 3 hours ago
Expires 1 month from now
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iqvia
Buenos Aires
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