Practical Clinical Manager with more than ten years of experience and background in clinical operations. Involved in active global clinical trials effectively partnering with Senior Project Managers on governance of Document Management, Start-upstudies, Sites Initiation, monitoring, and Close out visits and Phase IV(Neurology/CNS; Oncology; Cardiac; GI; Respiratory). Oversee project from feasibility to study close out, database of laboratories/vendors and forecast all costs. Tracking and submitting documents to central Institutional Review Boards. Training via Webinar and WebEx and provide systems access to staff (CRCs). Strong IT system validation. Liaison between US, Canada, and EU for Documents Management of Global Clinical Trials Studies. Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities.
0Implement new policies and educate staff on changes.
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