Clinical Research Associate

Há 3 dias


Belo Horizonte, Brasil beBeeClinical Tempo inteiro

Clinical Research Associate Role This role plays a pivotal part in shaping clinical trials, analyzing complex medical data, and contributing to the advancement of innovative treatments and therapies. Completes onsite and remote monitoring activities according to all ICH-GCP guidelines, applicable regulations, SOPs, and study processes. Verifies the protection of study participants by confirming informed consent procedures and protocol compliance with applicable regulations. Ensures the integrity of clinical data and that the study is conducted in accordance with approved protocol, GCP, applicable regulations, and SOPs. The ideal candidate possesses strong analytical and problem-solving skills, as well as excellent communication and interpersonal skills. Frequent travel is required (50-80%). Key Responsibilities Onsite Monitoring: Verify study sites and monitor trial conduct to ensure data accuracy and patient safety. Remote Monitoring: Conduct regular reviews of study data and site documentation to ensure compliance with regulatory requirements. Data Integrity: Ensure accurate and complete data collection, while maintaining the confidentiality of sensitive information. Requirements: Bachelor's degree in a relevant field (e.g., life sciences, public health). Minimum 1 year of experience in clinical research (on-site or remote monitoring, data management, or coordination). Strong understanding of ICH-GCP guidelines and regulatory requirements. Excellent communication and interpersonal skills. Familiarity with electronic data capture systems (EDCS) and other clinical trial technologies.



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