Clinical Research Associate

Há 2 dias


Porto Alegre, Brasil Bebeeclinicalresearch Tempo inteiro

Clinical research associates play a vital role in the success of clinical trials, ensuring that they are conducted efficiently and effectively.As a Clinical Research Associate with ICON, you will be responsible for designing and analyzing clinical trials, interpreting complex medical data, and contributing to innovative treatments.Job Responsibilities:Monitoring and Data Management: Completes onsite and remote monitoring activities in accordance with ICH-GCP guidelines and regulations, ensuring that all study-related documentation is accurate and complete.Participant Protection and Protocol Adherence: Verifies informed consent procedures and protocol adherence, ensuring that all participants are aware of the trial's objectives, risks, and benefits.Study Compliance and Site Management: Ensures study compliance with approved protocol, GCP, and regulations, managing site staff to facilitate trial deliverables and promoting a collaborative environment.Investigational Product Management: Verifies Investigational Product management, ensuring that all products are handled, stored, and distributed in compliance with regulatory requirements.Reporting and Communication: Writes and submits reports of site findings, communicating effectively with internal stakeholders and external partners to ensure seamless trial execution.This is a challenging role requiring strong analytical skills, attention to detail, and excellent communication abilities.As a Clinical Research Associate, you will play a critical role in the success of our clinical trials and contribute to the advancement of innovative treatments.



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