Salary for position Clinical Research Associate in Brazil

What kind of work does Clinical Research Associate typically do

• Conducting monitoring visits to clinical trial sites to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP).
• Reviewing and verifying study documentation including informed consent forms, source documents, and case report forms.
• Collaborating with site staff to facilitate the smooth execution of clinical trials.
• Providing training and support to site personnel on study protocols and procedures.
• Identifying and resolving issues related to study conduct and data integrity.
• Collecting and reporting adverse events and serious adverse events in accordance with regulatory guidelines.
• Maintaining accurate and timely records of monitoring activities and findings.
• Assisting in the preparation of study-related materials, including monitoring plans and reports.
• Ensuring proper storage and handling of investigational products.
• Participating in project team meetings and contributing to study progress discussions.