Edina-paróczai

Biography

Over twelve-year experience in clinical research both in pharmaceutical company and CROs, including 10 years as a clinical research associate (CRA) and two years as a LCRA / CTM back-up in international trials. Vast therapeutic experience in respiratory diseases, pulmonology, oncology, hematology, cardiology, diabetic, rheumatology, gastrointestinal, pediatrics and ophthalmology. Performing monitoring activities in studies from start-up / initiation to close-out phase. Acting as CTM in the clinical part of two trials (COPD and oncology trial) through start-up / activation period, maintenance and close-out period. Responsible for following up and escalating issues in EMEA, finalizing monitoring visit reports, newsletter / study manual. Proven leadership and communication skills with site staff including project/clinical team and sponsors. Participating at client / internal calls, leading country CRA calls. Experienced in different software like EDC, IXRS, e-Diaries, other study portals. Multiple vendors management experienced. Streamlined the process of sites initiation and activation. Experienced in study management in the maintenance period and close-out phase as well. Committed to achieve all project milestones within the agreed timeframe with enthusiasm and high quality and maintain the friendly, open-communication atmosphere in the study team.

Research Interest

ophthalmology