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04 years of experience on clinical research. Coordinator of clinical trials (phase II, III an IV).
Knowledge on GCPs, local regulatory submissions to Ethics Committees and IVRS and IWRS systems. Participation in meeting, monitoring, site initiation visits, trainning sessions and teleconferences with sponsors. Management of staff and training team members. Responsible for Feasibilities, all Start Up activities (including budget and contract negotiations). Engage and management of professional relationship with key opinion leaders (KOLs). Participation on continuing educational programs, meetings and programs for physicians. 

Advanced spoken/written/reading English. 
Basic spoken/written/r...

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