Georgios Lampadariou

4-month consultancy service that included successful creation of hazard logs, hazard catalogues (hazard registers), clinical authority to release/sign off on a number of clinical software products. The customer completed the project on time and within budget.

I successfully engaged and onboarded the QA team for the first time to include test plans for clinical safety logs/issues.

Registred nurse, intensive care and anesthetic recovery unit.

Integrated care pathways facilitator.

IT analyst/developer - integrated care pathways.

Infoflex clinical applications senior analyst/developer.

I lead our RWD/RWE discovery and data collection efforts and delivered 2 DTC (B2C) regulatory-approved research mobile products from ideation to launch and study execution.

I used study data collected through our products to ideate and offer new, Al-based product features.

Interviewed and hired team members from junior to director level.

Established SOPs for the product function in the company.

Established and maintained collaborations with industry and academic partners.

I managed our B2B patient portal solutions end to end.

Designed and implemented the company's first mobile app (patient portal) aligning web and mobile-first features.

Rebranded and developed a user engagement wellness tool for Bank of America employees.

Demonstrated our solutions to potential clients and conferences. My participation and demos to prospective customers at HIMMS 2017 resulted in the strongest leads of the event for our company, one with the American Heart Association and one with the American Association of Retired Persons (AARP) that were followed up by the sales team.

As the Lead Clinical Analyst for the EMEA region I worked with clients throughout the UK on clinical portal and clinical workstations (clinical context management) implementations.

Updated and expanded our business analysis tools to include mindmaps, flow diagrams, site maps and clickable wireframes.

Introduced high fidelity interactive prototypes to the UK customers (used Axure RP) to elicit and document requirements resulting in higher customer engagement.

As a result of the high-fidelity prototype success, I joined the pre-sales team and created interactive demos based on clinical scenarios defined by the prospective customers for tenders and proposals that jointly won multimillion-pound project contracts.

I relocated to Europe and spent time with family.

Applied and got accepted to medical school

I joined the company as a contractor at its early stages and set up product management processes and practices.

Managed the prioritization, design and implementation to successful MVP.

Conducted in-depth reviews of FDA guidance on adverse events and adverse events of special interest, identifying critical safety signals to integrate into study protocols.

Developed a comprehensive symptom cluster for adverse events associated with LSD administration in clinical trials, supporting robust safety monitoring and data interpretation.

Applied MedDRA dictionary coding standards to classify adverse events with precision ensuring consistency and accuracy in regulatory documentation.

Collaborated with MedDRA to develop an in-house query for adverse events of special interest for our psychedelic compounds (abuse potential) with a view to incorporate it into MedDRA as an Standardized MedDRA Query (SMQ).