+ Performing site selection, initiation, monitoring and close-out visits + Supporting the development of a subject recruitment plan + Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines + Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions + Collaborating with experts at study sites and with client representatives
**Qualifications:**
+ University degree in scientific discipline or health care + 2-4 years of independent on-site monitoring experience. + Very good computer skills including MS Office + Excellent command of Portuguese and English language. + Organizational, time management and problem-solving skills + Ability to establish and maintain effect...