Clinical Research Associate Professional

Há 10 horas


São Paulo, Brasil beBeeClinicalResearch Tempo inteiro

Clinical Research Associate Role Design and analyze clinical trials, interpret complex medical data, and contribute to innovative treatments. Verify study participant protection by confirming informed consent procedures and protocol adherence. Ensure clinical data integrity and compliance with approved protocols, GCP, regulations, and SOPs. Manage site staff to facilitate trial deliverables, such as subject enrollment and data delivery. Verify Investigational Product management and accountability. Submit reports of investigational site findings and update tracking systems. Escalate observed deficiencies, issues, and corrective actions. Manage essential documents according to local regulations and ICH-GCP guidelines. Perform risk assessments and management responsibilities throughout the project. The ideal candidate has a degree in a clinical or health-related field, healthcare professional licensure, and previous experience supporting clinical trials. Travel is required 50-80%. Competitive salary and benefits include well-being and work-life balance opportunities.



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