ARTHA Research

Clinical Research

• Prepare, review, and standardize clinical research technical documents (protocols, reports, regulatory materials), in Portuguese and English
• Support the structuring and maintenance of regulatory documentation for clinical studies, ensuring traceability, consistency, and compliance
• Prepare dossiers and conduct submissions to the Research Ethics Committee (CEP)
• Update and manage the Document Matrix for studies, ensuring organization, version control, and document governance
• Collaborate with Operational, Quality, and Statistical teams to ensure clarity, applicability, and integrity of documents
• Perform technical and linguistic review of scientific documents
• Support the analysis of scientific literature and the identification of methodologies applicable to studies
• Contribute to continuous improvement of documentation processes and internal standardization

Junior Document Analyst – Clinical Research