Full-stack data engineering, custom platform development and deep eCOA/ePRO expertise for life sciences, healthcare and regulated industries. Geneva-based. Globally deployed.
A rigorous, engineering-first approach to data problems — from greenfield platform builds and data pipeline architecture to deep clinical trial compliance work. Two complementary tiers: broad data systems expertise, and specialist eCOA/ePRO depth.
End-to-end platform development, data infrastructure and custom tooling for any data-intensive domain.
Design and build of custom web platforms, internal tools and data management systems. Full stack — from database schema to deployed interface.
Ingest, transform, validate and deliver data across formats — SQL, XML, SAS, ASCII, JSON. Inbound and outbound integrations with third-party APIs.
Eliminate manual bottlenecks. Build generation tools, deployment automators and report factories that shrink days-long cycles to minutes.
Custom dashboards, email alerts, data quality monitoring and audit-ready reports tailored to your workflow and stakeholders.
Docker-based deployments, Linux VPS management, NGINX/Traefik routing. Reliable, reproducible environments from staging to production.
Connect disparate systems and vendors. Experience integrating third-party health device APIs into regulated clinical data flows.
Deep domain expertise in electronic Clinical Outcome Assessments across the full trial lifecycle, from protocol to database lock.
Nine years building, managing and automating eCOA/ePRO systems for global Phase II–IV trials. My work spans database architecture, CDISC/SDTM compliance, sponsor data delivery and regulatory audit support — with deployment across 45+ countries and 20,000+ patients, for sponsors including Novartis, Roche, Pfizer, GSK and argenx.
Design and build of clinical outcome assessment databases in Microsoft SQL Server, aligned to study protocol and sponsor DTA requirements.
MS SQL Server · PL/SQLElectronic COA data mappings to CDISC standards. Internal SDTM metadata reporting and DTA implementation from Data Transfer Specifications documents.
CDISC · SDTM · SASCustom SAS, ASCII and XML data transfers per sponsor DTA. Automated DTS document generation from JSON study design inputs.
SAS · XML · ASCIILed the build of an internal platform that cut eCOA database deployment time from 4 hours to 30 minutes — QA to Production, with metadata extraction and permission controls.
DevOps · JavaScript · SQLSQL-based data quality checks and edit check development for verification prior to data transfer. Reducing discrepancy rates ahead of database lock.
SQL · Data QCSOP authoring for project management departments. Audit support for FDA and EMA regulatory reviews. Compliance documentation throughout the trial lifecycle.
FDA · EMA · SOPFrom academic physics research to data engineering leadership in global clinical trials.
Full-stack platform development for a Swiss home-care startup delivering medical services for elders and people with disabilities.
Creator of trialsmap.com — a clinical trial discovery engine aggregating recruiting studies from FDA, EMA and WHO registries.
Clinical data capture consultancy for universities and research institutions.
Led design and development of an internal web deployment platform for eCOA databases (QA → Production), cutting cycle time from 4 hours to 30 minutes. Managed a team of 3 developers.
Built an automation tool reducing eCOA database build time from 2 days to 2 hours — widely adopted across Data Delivery and Data Management teams.
Developed 50+ clinical databases for Novartis, Roche, Pfizer, GSK and argenx. Delivered custom data transfers, analytics dashboards and third-party API integrations.
Managed 14 concurrent eCOA projects from kickoff through FPI/SIV to database lock. Studies across 45+ countries, targeting 20,000+ patients, with multi-million dollar budgets.
Primary sponsor liaison for GSK, Idorsia, Roche and Alvothech. Internal liaison across software, operational and data management teams. Drafted and maintained departmental SOPs.
Teaching assistant for calculus, algebra and geometry. Management of industrial and academic research projects applying graphene in practical engineering contexts.
Doctoral research in condensed matter physics. Rigorous quantitative training underpinning a data-first approach to complex systems — from experimental design through statistical analysis.
Platforms and tools built independently — solving real problems in healthcare access, practice management and Swiss finance.
Clinical trial discovery engine aggregating recruiting studies from FDA, EMA and WHO registries. Designed to reduce the barrier between patients and relevant research. Beta finalising.
→ trialsmap.comFull CRM and administration platform for a Swiss dental clinic — patient records, appointment management and billing workflows in a single integrated system.
→ hybumad.chSwiss QR bill generation service for individuals with Swiss bank accounts and SMEs. Compliant with Swiss payment standards. Work in progress.
→ mafactureqr.chAutomated extraction and classification of financial data from bank statements (XML, CSV) into WinBiz-compatible Swiss accounting formats. Deployed at small Swiss enterprises for year-end accounting acceleration.
Available for data engineering mandates, clinical database projects, eCOA/ePRO consulting and digital healthcare platform development. Typically engaged by sponsors, CROs, startups and research institutions.
Based in Geneva — working remotely across Europe and globally.