Research Associate Professional

Há 5 dias


Brasília DF, Brasil beBeeClinical Tempo inteiro

Job Title: Contract Clinical Research Associate Job Description: We are seeking a detail-oriented and experienced professional to monitor and manage Phase 2 Seizure study clinical trials. The ideal candidate will ensure the trial is conducted in compliance with regulatory standards, Good Clinical Practice (GCP), and the study protocol. Required Skills and Qualifications: Site Management and Monitoring: Conduct site qualification, initiation, interim monitoring, and close-out visits to ensure proper site adherence to protocols, GCP, and regulatory requirements. Regulatory Compliance: Ensure all clinical trial documentation is maintained according to regulatory guidelines. Review informed consent documents and confirm proper consenting procedures. Safety and Data Management: Monitor and report adverse events (AEs), serious adverse events (SAEs), and dose-limiting toxicities. Collaboration and Communication: Build and maintain relationships with study investigators and site staff. Communicate study updates and findings to internal teams. Benefits: The successful candidate will have the opportunity to work on complex clinical trials, develop their skills in site management and monitoring, and contribute to the success of the project.



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