Senior Trial Manager

Há 4 dias


Manaus, Brasil Bebeeclinicalresearchassociate Tempo inteiro

Contract Clinical Research AssociateThe clinical trials industry requires highly skilled professionals to manage and monitor research studies.As a Clinical Research Associate (CRA), you will play a pivotal role in ensuring the success of Phase 2 Seizure studies.Develop a thorough understanding of regulatory standards, Good Clinical Practice (GCP), and study protocols to ensure site compliance.Verify data accuracy and ensure timely submissions to regulatory teams.Collaborate with site personnel to conduct monitoring visits, including qualification, initiation, interim, and close-out visits.Key Responsibilities:Site Management and Monitoring: Conduct regular site assessments to ensure adherence to GCP guidelines.Regulatory Compliance: Ensure all clinical trial documentation is accurately maintained according to regulatory requirements.Safety and Data Management: Monitor and report adverse events, serious adverse events, and dose-limiting toxicities.Successful candidates for this position should possess a degree in Life Sciences or a related field, with at least 2-4 years of experience as a Clinical Research Associate in oncology trials.



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