frasersimpson

Providing product strategy and investment advisory services to healthcare, technology, and investment clients. Delivered healthcare market entry strategy for AI privacy platform, including regulatory assessment, product-workflow fit analysis, stakeholder mapping, competitive positioning, and pilot design framework Produced go/no-go analysis for decentralised scientific journal launch, defining journal models, governance structures, trust frameworks, and credibility roadmap Sourcing deal flow and conducting due diligence for early-stage technology investments, producing market assessments and investment analysis Contributing to investment fund development across thesis formulation, client relationships, and operational framework design

Led technical product development for clinical guideline products serving 45,000+ global members across multiple regulatory jurisdictions. Launched 9 regulatory-compliant clinical guideline products serving 400,000+ healthcare professionals across international markets, managing 6-month development cycles and achieving 2.8m+ downloads Coordinated 50+ senior clinical stakeholders across international markets, navigating conflicting regulatory requirements, treatment availability variations, patient demographic representation debates, and pre-publication data constraints Built operational infrastructure, including SOPs, technical documentation and training programmes for 15+ team members across 3 departments Advocated product roadmap priorities to executive leadership and advisory boards, securing resource allocation for user-driven feature development

Co-developed quarterly medical journal with CEO and delivered medical writing services for medical communications agency. Designed product roadmap and feature prioritisation framework for peer-reviewed medical journal, integrating user feedback systems and shifting company focus toward product-led development Delivered quarterly journal editions achieving 30% QoQ submission growth through systematic positioning strategy and market development Ghostwrote 4 peer-reviewed articles for journal publication and produced 3 industry reports booklets for healthcare professionals Delivered AAQ-accredited training programme, achieving 90% satisfaction score

Delivered medical writing services and implemented user feedback systems to improve product quality for boutique Swiss medical communications agency. Produced 25 reports across 4 product lines through clinical trial data analysis and 12 expert interviews, delivering industry updates for healthcare professionals Wrote technical marketing content and promotional materials across 6 pharmaceutical products, securing 85% client retention through quality delivery Implemented user feedback collection and analysis framework where none existed, integrating client insights into product development and improving satisfaction scores

Designed and executed multi-year translational oncology research programme, coordinating international collaborators across complex regulatory requirements. Led 4-member team through 4 concurrent research projects across 5 nationwide sites, coordinating 20+ international stakeholders and managing competing priorities against regulatory requirements Secured 150,000 CHF in competitive research funding across 2 successful grant applications, translating complex technical concepts and impact to funding bodies Developed 11 regulatory-compliant SOPs standardising processes across 3 research teams, achieving 40% reduction in protocol deviations Conducted multi-modal experimental and statistical analyses across biological samples using Matlab, GraphPad and R, validating research hypotheses Delivered technical training programmes and performed peer review for 9 scientific publications Presented research findings at 7 international conferences, winning 3 awards