Position Overview
Clinical Research Associate
Your responsibilities will include:
Performing site selection, initiation, monitoring and close-out visits after completing training periodSupporting the development of a subject recruitment planEvaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelinesManaging progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutionsCollaborating with experts at study sites and with client representatives
Qualifications:
University degree in scientific discipline or health careRequires at least 1 year of on-site monitoring experience. Very good computer skills including MS OfficeExcellent command of Portuguese and English languageOrganizational, time management and pro...