Clinical Trial Manager

Há 9 horas


Recife, Brasil Bebeeresearch Tempo inteiro

We are currently seeking a skilled Clinical Research Associate to oversee and manage Phase 2 Seizure study clinical trials.The successful candidate will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol.Key Responsibilities:Site Management and Monitoring: Conduct site qualification, initiation, interim monitoring, and close-out visits.Regulatory Compliance: Maintain all clinical trial documentation according to regulatory guidelines.Safety and Data Management: Monitor and report adverse events (AEs), serious adverse events (SAEs), and dose-limiting toxicities.A career as a Clinical Research Associate is an exciting opportunity for those who enjoy working in a fast-paced environment, collaborating with cross-functional teams, and staying up-to-date with the latest developments in the pharmaceutical industry.To be successful in this role, you should have excellent communication skills, attention to detail, and experience working in clinical research or a related field.Additionally, you should be able to work independently and as part of a team, prioritizing tasks and managing multiple projects simultaneously.



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