Clinical Research Associate
Your responsibilities will include:
Performing site selection, initiation, monitoring and close-out visitsSupporting 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 careMinimum oftwo-four years of on-site monitoring experience alternatively an equivalent combination of education, training and experienceVery good computer skills including MS OfficeExcellent command of Portuguese and English...