Clinical Research Associate I

ICON · Sao Paulo, Brazil

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Clinical OperationsFull-timeCompany career page

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Role summary

Clinical Research Associate I position at ICON in São Paulo supporting sponsor-dedicated clinical trial operations. The role involves study monitoring, coordination, documentation, and stakeholder management while ensuring regulatory compliance and patient safety in a collaborative environment.

What they're looking for

University degree in medicine, science, or equivalent field
Knowledge of ICH-GCP guidelines and ability to review medical data
Fluent written and verbal English communication
Strong interpersonal skills for timely stakeholder query resolution
Willingness to travel approximately 60% as required
Legal authorization to work in Brazil

What you'll be doing

Coordinate study setup and monitoring activities with accurate reporting and documentation maintenance
Process sponsor-generated queries efficiently and manage study cost control
Prepare and review study documentation and feasibility assessments for new proposals
Build and maintain collaborative relationships with investigators, site staff, and sponsors
Ensure compliance with protocols, regulatory requirements, and patient safety standards

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Date posted5 days ago

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