Senior Clinical Trial Specialist

Há 3 dias


Brasília, Brasil beBeeClinical Tempo inteiro

Design and Analyze Clinical Trials Key Responsibilities Conduct onsite and remote monitoring activities in compliance with ICH-GCP guidelines, regulations, SOPs, and study processes. Verify the protection of study participants by confirming informed consent procedures and protocol adherence to applicable regulations. Ensure the integrity of clinical data and that studies are conducted in compliance with approved protocols, GCP, regulations, and SOPs. Requirements Bachelor's degree or international equivalent in a clinical, science, or health-related field from an accredited institution. Healthcare professional licensure, i.e., registered nurse. Prior experience supporting clinical trials, including solid onsite monitoring experience in CROs or pharma companies. Remote work is available but 50-80% travel is required.



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