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Há 5 horas

Fortaleza, Brasil beBeeClinicalResearch Tempo inteiro

Job Title: Clinical Research Associate As a diligent and experienced Clinical Research Associate, you will oversee the execution of Phase 2 clinical trials ensuring compliance with regulatory standards, Good Clinical Practice (GCP), and study protocol. Collaborate with investigators, site personnel, and cross-functional teams to guarantee participant safety and well-being. Responsibilities: Study Management : Monitor and manage trial sites, ensuring timely completion and data accuracy. Regulatory Compliance : Maintain adherence to GCP guidelines, FDA regulations, and ICH principles. Safety and Data Management : Oversee participant safety and ensure accurate data collection and management. Collaboration and Communication : Foster effective collaboration among stakeholders to achieve trial objectives. Qualifications: Bachelor's Degree in Life Sciences or related field required. At least 2-4 years of experience as CRA in oncology trials preferred. Strong Knowledge of GCP, FDA Regulations, and ICH Guidelines essential. Experience with electronic data capture systems and clinical trial management systems advantageous. Preferred Qualifications: Previous experience in early-phase oncology trials desirable. Strong Understanding of Pharmacokinetics and Pharmacodynamics Assessments beneficial.

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