Sarolta Tabor

As a Senior Clinical Data Scientist at Parexel, I led data management initiatives, achieving a 40% reduction in data quality issues and a 35% decrease in open queries. My role involved proactive communication on data management topics, risk assessment, and collaboration with cross-functional teams to ensure data integrity and timely project deliveries.

In my role as Lead Data Manager at ICON, I oversaw multiple clinical studies, ensuring 100% audit readiness and 95% timeline adherence. I provided leadership to data managers, managed study files, and facilitated cross-functional presentations to meet project milestones.

As a Data Team Lead at IQVIA, I guided the creation of systems to ensure clinical data integrity and managed project resources. My responsibilities included leading data managers, maintaining audit-ready study files, and collaborating with cross-functional teams to implement CDM processes.

In my position as a Remote Site Monitor at PPD, I was responsible for site monitoring, initiation, and close-out activities. I managed drug supply and query management to ensure compliance and quality throughout the study lifecycle.

As a Project Manager in Data Management at Auxiliis Pharma, I oversaw study start-up, maintenance, and close-out processes. I managed a team of six direct reports and ensured compliance through internal and external audits while maintaining project quality and budget.

In my role as Manager of the Clinical Trial Team at Tata Consultancy Services, I managed safety processes and SOPs, assisted in signal detection, and led audits including MHRA and FDA. I also oversaw a team of 15-20 direct reports, ensuring compliance and quality in pharmacovigilance activities.

Completed an Associate of Applied Science in Medical Laboratory Technologies, gaining foundational knowledge and skills in laboratory practices, procedures, and technologies essential for clinical settings.