Ana Carolina S.

Biomedical professional with over 8 years of research experience including pre-clinical and clinical trials. I focus on optimizing clinical trial processes, supported by a track record in site billing (supported by EDC and CTMS), account receivable (AR; using QuickBooks), site payments and contracts management, document management, administrative support and stakeholder coordination. Proficient in ICH-GCP guidelines, CTMS, Microsoft Office Suite, and project communications, I contribute to ensuring that project activities adhere to quality standards and regulatory guidelines. In addition to my technical expertise, I'm a multilingual professional, native in Portuguese and fluent in English and Italian, fully dedicated to achieving excellence in clinical research. Career Highlights • Efficient Processing: Reduced contract processing time by 20% stablishing trackers, ensuring transparency and stakeholders satisfaction. • Effective Communication: Acted as point of contact for study payments and contracts, increasing satisfaction among stakeholders in 50%. • Document Management: Cut access and update time for critical documents on TMF by 40%. • Data Integrity: Maintained data quality in clinical platforms, ensuring compliance and reducing the need for source sponsor's documents correction requests in 40%.