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Clinical Research Associate

Skills

GCP

Description

The Clinical Research Associate is responsible for managing and monitoring clinical trials to ensure they are conducted in compliance with study protocols, ICH-GCP, and applicable regulations.

This includes site selection, initiation, monitoring, and close-out activities, while ensuring data quality and patient safety.

The role reports to the Clinical Project Manager.

Key

Responsibilities

Identify, assess, and initiate investigational sites Conduct feasibility, pre-study, initiation, monitoring…

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