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Clinical Trials Specialist
2 weeks ago
Job Overview
The position of Clinical Research Associate is available at our organization. The role involves analyzing and creating clinical trial documents.
This job requires the ability to work in a fast-paced environment and maintain compliance with global regulatory standards (FDA, EMA, ICH-GCP). Knowledge of medical terminologies and ontologies is also necessary.
The ideal candidate will have a strong understanding of clinical trials and the ability to analyze and author clinical trial documents.
Responsibilities: