Job Details

A company is looking for a Source Document Specialist who is responsible for ensuring accurate, compliant, and efficient clinical trial documentation.Key ResponsibilitiesPrepare and develop accurate source documents based on clinical trial protocols, ensuring compliance with relevant regulationsReview and validate source documents for completeness and accuracy, coordinating with site staff and internal teamsMaintain version control and implement protocol amendments efficiently while ensuring compliance with regulatory requirementsRequired Qualifications, Training, and EducationBachelor's degree in a health-related field preferred, or equivalent work experience in clinical researchMinimum of 2 years of experience in clinical research, preferably as a Clinical Research Coordinator or in a similar roleStrong knowledge of clinical trial operations, GCP guidelines, and regulatory complianceProficiency in Microsoft Excel, Word, SharePoint, and other digital documentation toolsFluency in Portuguese and English for effective communication and documentation