Pavel Lostak

• Contributing to Process Redesign Efforts • Harmonizing and Optimizing Processes by challenging traditional Way of doing things, Eliminating Waste, Error and Rework and Developing Solutions

Responsible for overseeing*** all supporting systems and services supplied centrally to local clinical trial teams with liason to local and corporate IS/IT departments. Included not limited to: • CTMS (data mapping within different CTMS, database deduplication) • EDC (internal/external) - eCRF database preparation • Reporting Tools (user need analysis and design) • Collaborative *** = training, support, analysis of best practices with electronic programs used in Clinical Research on local / region

• Monitoring and reporting studies in compliance with ICH GCP in various therapeutic areas • eCRF Studies: training and coordination (CSU/CRU and investigator's site staff), intranet presentation for Czech CSU/CRU • Diagnosistic areas: • IIIA/IIIB – Pediatrics/Diabetics (Diabetes Mellitus – type I), Oncology (Pancreatic Cancer), Pediatrics/Musculo Skeleton (Osteogenesis Imperfecta), CNS (Insomnia), Cardiovascular (Thrombosis), IIB – Gastroenterology (Ulcerative Colitis)

• Prescription drugs expedition, documentation, administrative

• English scientific text processing and its presentation

Pharmacology, Chemistry, Statistics and Informatics