- Support Data and Insights team’s initiatives, provide project management and oversight;- Support projects initiation, track project execution, financials, budgets, etc.- Assist in the due diligence of new real world data providers/vendors and drive RWD quality assessments to inform investment decisions- Document RWE requests and track progress toward project completion, project metrics and business goals;- Establish information sharing forums to share project updates and to educate colleagues throughout the organization on RWE enabled use cases and best practices- Communicate and advocate effectively throughout the organization to support the appropriate use of RWE;- Educate colleagues throughout the organization on RWE enabled use cases and best practices- Proactively identify opportunities for greater use of RWE across the organization- Serve as primary project contact with RWD data provider to ensure communication is maintained and reporting schedules are adhered to.- Collect information on team performance against contract, customer expectations, and project baselines.- Lead problem solving and resolution efforts to include management of risk, contingencies and issues.- Prepare and present project information at internal and external meetings.- Mentor interns / lead tech teams to address key business challenges.

- Crafted and delivered analytical reports, dashboards, and presentations to empower data-driven decision-making across the organization.- Strategized and executed data extraction and exploration methodologies aligned with business objectives and modeling requirements, utilizing diverse datasets from internal, real-world, and external resources.- Contributed to the coding and integration of data sources for advanced modeling and simulation techniques.

In-silico clinical trials / virtual patients initiative: Overall objective: use of patients-level data from past clinical trials & RWD to generate virtual cohort of patients through copula method & use of AI models to predict endpoints in these virtual patients and then present the results through an interface where the end-user can play with inclusion/exclusion criteria & see impacts on the different virtual clinical trials simulated.- Applied on both neurology & oncology use cases- ISCT interface point of contact for updates & presentation of simulations results to end-users, creation of visuals & contribution to the regular touchpoints to gather stakeholders' insights to improve the models and enable simple communication between data scientists & medical directors.- Dashboard creation & real-world data exploration

- Data Management daily activities :. Set-up : creation of the Data Validation Plan (DVP) & the CRF completion guideline, UAT (User Acceptance Testing) in DEV environment…. On-going studies management : outsourcing activities coordination (ex : change order), queries’ monitoring & data quality review throughout the conduct of the studies . End-of-study tasks : final cleaning before DB lock, blind data review preparation…- Reflections on a new macro for data cleaning (Data Quality Review / Risk-based monitoring) : new types of listings / new indicators for the cleaning of the database during the conduct of the study --> dates order, missing values on the primary outcome, drop-out subjects follow-up- Thinking on the use/relevance of the Edit-Checks (EC) : comparison between several studies (proportion of standard/non-standard EC, amount of time each EC fired / site…)

- Creation of a Clinical Metadata Catalog : implementation of all the studies’ metadata (clinical metadata database) / integration and cleaning of a part of the operational metadata (operational metadata database) : Process based on CDISC-SDTM Implementation Guide Sections 6 and 7 and Visualization with TIBCO Spotfire®- Role in an on-going clinical study management : queries’ creation and follow-up, SAS reports’ creation- Contribution to a study setting up : checking of the clinical design, creation of the DVP, validation of certain validation’ protocoles (= UAT as tester)

- Preparing of quality indicators and external audit- Checking of Physician Financial Transparency Reports (Sunshine Act) for different partners (Janssen Cilan, Mylan Medical, Chiesi, Daiichi Sankyo, Nestlé, Urgo)- Tracking of medical questions, quality claims and postmarketing surveillance case reports

Summer Session – ESL program (English as a Second Language) in order to prepare the TOEIC exam and to improve my linguistic skills6 weeks session with those courses : English as a Second Language, Academic Vocabulary and Writing ExpressionTOEIC Score at the end of the session : 860TOEIC Score in Feb. 2016 : 895

- Collection of the Sunshine Act reports linked to the new regulations- Follow-up of the post-marketing surveillance cases