Contract Coordinator - FSP RSU Team

IQVIA · São Paulo, Brazil

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Clinical OperationsFull-timeCompany career page

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Role summary

Contract coordinator supporting site activation activities for clinical trials at IQVIA's São Paulo office. Role involves preparing regulatory documents, coordinating with study sites and internal teams, and maintaining project tracking systems under general supervision.

What they're looking for

3+ years experience in administrative environment or equivalent
Knowledge of regulatory document preparation and review
Familiarity with clinical trial site activation processes
Proficiency with databases and project tracking tools
Strong attention to detail and documentation accuracy

What you'll be doing

Perform site activation activities for assigned clinical studies per regulations and SOPs
Prepare and review regulatory documents for completeness and accuracy
Distribute completed documents to sites and internal project stakeholders
Update and maintain project databases, tracking tools, and timelines
Track progress and follow up on regulatory and ethics document approvals

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Date posted1 day ago

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