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Há 7 dias

Ituiutaba, Brasil Bebeeclinicalresearch Tempo inteiro

Phase 2 Clinical Trials CoordinatorThis role involves overseeing and managing Phase 2 clinical trials, ensuring adherence to regulatory standards and Good Clinical Practice (GCP).Key responsibilities include site qualification, initiation, interim monitoring, and close-out visits, as well as verifying accurate data collection and reporting.Regulatory Compliance: Guarantee that all clinical trial documentation is maintained in accordance with regulatory guidelines.Safety and Data Management: Monitor and report adverse events, serious adverse events, and dose-limiting toxicities.Requirements:Bachelor's degree in Life Sciences, Nursing, or a related field.A minimum of 2-4 years of experience as a Clinical Research Associate in oncology trials.

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