Kons Kushnir
Clinical Research Associate @Teva Pharmaceuticals
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WORK HISTORY
Clinical Research Associate @Teva Pharmaceuticals
Worked on therapeutic areas of ENT and Neurology·Initiated sites by assessing the qualification of potential investigative sites·Initiated studies, instructed site personnel on the proper conduct of studies, to review data and ensure accuracy of data collected and to terminate studies ·Monitored study sites·Provided regular clinical status information to team members and project management ·Performed source document verification, retrieved Case Report Forms (CRFs) and performed query resolution in a timely manner and performed drug accountability and safety at investigative sites ·Performed investigative site file reconciliation and requested for required documents and make sure they compliance with appropriate local regulatory requirements, ICH guidelines, project Standard Operating Procedures (SOPs), and sponsor requirements ·Ensured SAEs and deviations reported to IRB·Resolved queries·Ensured deviations and SAEs reported to IRB·Responded to requests from investigative sites in a timely fashion Served as a resource for and interacted with other functional areas to resolve site issues and facilitated project timelines
EDUCATION
Medical University of Lublin
Doctor of Medicine - MD
ABOUT KONS KUSHNIR
Over 9 years of experience in the Clinical Research Industry ·Working knowledge and…
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