Maarten Knaepen Email & Phone Number

Hasselt, Flemish Region, Belgium

I contribute to making urban life smarter and more enjoyable through data-driven solutions. My work involves analyzing complex datasets, designing predictive models, and developing scalable algorithms that power innovative smart city applications. From optimizing traffic flows to monitoring air quality and noise pollution with sensor data, I help transform raw data into actionable insights that improve city living for citizens.

Brussels Region, Belgium

Successfully completed a project to extract film metadata from public events and then enrich that metadata to improve the recommender system

Brussels Hoofdstedelijk Gewest, België

As a student of BeCode's Pedagogical Framework for AI & Data Science program, I developed a robust, hands-on skillset at the cutting-edge of these transformative technologies. Through intensive coursework and collaborative projects, I gained expertise in:- Applying advanced Python programming and popular data science libraries like NumPy, Pandas, and Scikit-Learn- Building and deploying machine learning models for classification, regression, and clustering tasks- Cultivating a nuanced understanding of AI ethics, bias, and responsible development principles- Experiencing innovative, engaging instructional methods designed to empower learners- Honing my ability to ideate, prototype, and present data-driven solutions as part of cross-functional teams- With this unique blend of technical acumen and pedagogical best practices, I'm eager to leverage my BeCode experience to drive innovation and democratize access to transformative AI/data capabilities.

België

Oversee the implementation of the Clinical Metadata Repository system (CMDR) for clinical trials.Utilize UCB's strategic decisions and standard libraries to create study-level materials such as:Basic eCRF forms, instructions, and edit checksData transfer specifications for clinical data collected outside eCRFSDTM datasets and RAW to SDTM mappingsCoordinate with UCB colleagues and CRO partners to align on timelines for designing and implementing EDC solutions.Collaborate with Study Data Leads to plan data receipt and ensure data quality throughout trials.Lead the process of loading data from various sources into clinical and operational data repositories, addressing any issues that arise.Data sources may include strategic partners, vendors/CROs, central labs, imaging vendors, and other relevant sources for clinical trials.

Kyiv Metropolitan Area

Oversee the implementation of the Clinical Metadata Repository system (CMDR) for clinical trials.Utilize UCB's strategic decisions and standard libraries to create study-level materials such as:Basic eCRF forms, instructions, and edit checksData transfer specifications for clinical data collected outside eCRFSDTM datasets and RAW to SDTM mappingsCoordinate with UCB colleagues and CRO partners to align on timelines for designing and implementing EDC solutions.Collaborate with Study Data Leads to plan data receipt and ensure data quality throughout trials.Lead the process of loading data from various sources into clinical and operational data repositories, addressing any issues that arise.Data sources may include strategic partners, vendors/CROs, central labs, imaging vendors, and other relevant sources for clinical trials.

Kyiv City, Ukraine

Responsible for training 3 new colleagues in basic EDS (electronic data specialist) tasks, assigned workloads and respected deadlines.Reviewed data discrepancies generated by edit checks for external data and performed subsequent query management to resolve issues.Assisted with review of external data edit checks, validated electronically transmitted data. Entered and performed QC for local laboratory normal ranges.Communicate problems involving data transfers, data point issues and validation issues to vendors and clients.

Kiev Region, Ukraine

Experienced with SDTM and able to implement maintain and ensure strict compliance with CDISC or client-specific SDTM standards.Created and reviewed CDISC complient programming specifications.Created and reviewed SDTM compliant annotated CRF's.

Master'S Degree, Biomedische Wetenschappen (Biomedical Sciences)

Higher education focused on development of new medicines, clinical trials and gcp, origin and treatment of diseases. Minor in Quality.

Bachelor'S Degree, Biomedical Laboratory Technology

Obtained certification to become laboratory technologist. Experience with hematological, immunological and microbiological laboratory.