About Hana
French
Native or bilingual
English
Fluent
Experience
- Tamer Healthcare (TAAM)Data Scientist (Clinical & Healthcare Supply Chain)April 2025 - Today (1 year and 4 months)Riyadh Saudi Arabia• • Deliver end-to-end analytics to support Clinical and healthcare supply chain decision-making for major clients including Health Holding Company (HHC) and King Faisal Specialist Hospital & Research Centre (KFSHRC).• • Develop data-driven inventory and procurement analyses (consumption patterns, stock risks, order recommendations) to improve operational visibility and performance.• • Build Streamlit applications to automate reporting workflows and enable faster, self-service insights for stakeholders.• • Design Power BI dashboards to monitor Clinical and supply chain KPIs and communicate performance trends to business and operational teams.• • Develop NLP-based matching and classification solutions to improve master data quality and reduce manual effort.• • Prepare and present analytical results, project updates, and recommendations to cross-functional stakeholders, ensuring clarity and actionable outcomes
- BraincellData AnalystNovember 2024 - May 2025 (6 months)Riyadh Saudi Arabia• • Analyzed datasets and delivered structured reporting to support decision-making and operational performance.• • Built dashboards and KPI tracking to monitor performance and highlight trends, risks, and improvement opportunities using FineBi• • Performed data cleaning, validation, and standardization to improve reliability and usability across multiple sources.• • Collaborated with stakeholders to translate business needs into actionable insights and clear analytical outputs
- ICON plc (Clinical Research Organization)Clinical Research Site Manager (Clinical Data & Quality Focus)February 2022 - October 2023 (1 year and 8 months)Paris, France• • Ensured clinical data quality and integrity through continuous site monitoring and data reviews, in compliance with Good Clinical Practice (GCP) standards.• • Reviewed Case Report Forms (CRFs) and source documentation to identify inconsistencies, missing data, and protocol deviations, ensuring accurate and reliable reporting.• • Coordinated regulatory documentation submissions and follow-up with Ethics Committees (IRB/EC), ensuring completeness, traceability, and audit readiness.• • Led site initiation, routine follow-up, and issue management activities to support correct study execution and timely resolution of queries.• • Maintained structured documentation and clear stakeholder communication to support clean data collection and reliable study outcomes
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Education
- Data Scientist & AILeWagon-Marseille2024Data Scientist & AI
- Msc Biobanks & Complex Data ManagementUniversité Nice Côte d'Azur2020