Clinical Trials Specialist

Há 2 dias


Porto Alegre RS, Brasil beBeeClinicalResearchAssociate Tempo inteiro

Key Responsibilities: Monitor and manage clinical trials. Ensure site compliance with regulatory requirements. Verify accurate data collection and reporting. Evaluate site performance and implement corrective actions as needed. About the Ideal Candidate: A Bachelor's degree in Life Sciences, Nursing, or a related field is required. At least 2-4 years of experience as a Clinical Research Associate (CRA) in oncology trials is preferred. Strong knowledge of Good Clinical Practice (GCP), FDA regulations, and ICH guidelines is essential. Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS) is also required. Job Summary: We are seeking an experienced Clinical Research Associate to join our team. As a CRA, you will be responsible for monitoring and managing clinical trials, ensuring site compliance with regulatory requirements, and verifying accurate data collection and reporting.


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