About Marie Gabrielle
I am a physician specializing in Internal Medicine with 20 years of clinical practice. My professional expertise lies in the "translational bridge"—the ability to convert complex laboratory measurements into meaningful clinical, safety, and regulatory decisions. As an International Regular Member of the American Society of Pharmacology and Experimental Therapeutics (ASPET), I provide an elite, end-to-end perspective on the entire drug development lifecycle.
The Foundation: Laboratory Science & Clinical Investigation
- Early-Phase Diagnostics: Proof-of-concept metabolic studies (e.g., 1,5-anhydroglucitol).
- Safety Assessment: Thorough QT/QTc exposure–response studies correlating ECG findings with plasma drug concentrations.
- PK Characterization: Randomized crossover studies determining Cmax, Tmax, AUC, and clearance.
Data-Driven Clinical Strategy & Authorship
English
Native or bilingual
Spanish
Fluent
Filipino
Native or bilingual
French
Basic
Russian
Basic
Experience
- C2Space Tech LLCResearch and Operations LeadAVIATION AND AEROSPACEApril 2026 - Today (3 months)Houston, United States- Lead research operations and cross-functional coordination for projects focused on human performance and safety in high-consequence environments (bioastronautics, aerospace and extreme conditions).- Oversee the development, review, and optimization of clinical and experimental protocols, ensuring alignment with regulatory, ethical, and scientific standards (IRB-ready).- Serve as the central liaison between multidisciplinary teams including physicians, engineers, legal/regulatory partners, and international collaborators.- Design and refine operational workflows to support efficient execution of research studies, including coordination of external vendors, CROs, and technical partners.- Provide clinical expertise in human physiology, functional performance, and risk mitigation under extreme environmental stressors.- Support strategic initiatives by translating complex medical and scientific requirements into structured, scalable systems and processes.- Integrate data-driven approaches and digital tools (including AI-assisted workflows) to enhance research design, data handling, and decision-making.- Manage communications, documentation, and timelines across multiple concurrent projects in a fast-paced, high-stakes environment.
- Eurawest TechnologiesDirectorJanuary 2025 - Today (1 year and 6 months)Sofia, BulgariaElite Digital Health Agency: Lead a full-service digital marketing and IT organization specialized in the global MedTech and healthcare sectors, serving as the European sister company to Eternus Global.Medical Digital Advertising: Drive market dominance for health clients through specialized PPC (Pay-Per-Click), SEO, and comprehensive digital growth strategies.Health Medical Cybersecurity: Implement robust, HIPAA/GDPR-compliant security frameworks for medical devices and health information systems, focusing on threat modeling and risk mitigation.Translational KPO Services: Provide high-end Medical Knowledge Process Outsourcing (KPO), including regulatory-compliant medical writing and biostatistical analysis for global pharma and biotech firms.Market-Entry Strategy: Guide international medical brands through complex European regulatory landscapes (EMA/GDPR) to ensure successful cross-border market entry.Full-Stack Health Tech: Oversee the development of secure, scalable web and mobile applications tailored for clinical environments and patient-facing digital health services.Branding for Life Sciences: Execute evidence-based branding and communication strategies that translate scientific excellence into compelling market narratives.Data-Driven Growth: Leverage background as a physician and data scientist to deliver biostatistical insights that optimize digital advertising ROI for pharmaceutical clients.
- SNBL - INAClinical InvestigatorPHARMACEUTICALS INDUSTRYNovember 2010 - December 2014 (4 years and 1 month)Ina, JapanPhase I/II Clinical Leadership: Led combined Phase I and II clinical trials for both investigational drugs and functional food products.Regulatory Bridging: Expert in ICH GCP with a specialized focus on harmonizing Japanese (PMDA) and European (EMA) regulatory standards, supported by SNBL’s international presence.Principal Investigator (1,5-AG): Directed Phase I/II efficacy and safety studies for 1,5-Anhydroglucitol in diabetic populations to assess metabolic outcomes.Biomarker Validation: Established 1,5-AG as a precise clinical biomarker for tracking short-term glycemic variability and postprandial glucose excursions.Cardiovascular Safety (Sub-I): Conducted Thorough QT/QTc (TQT) exposure-response studies specifically for the safety profiling of quinolone antibiotics.PK/PD Precision: Managed rigorous sampling and timing protocols to correlate plasma drug concentrations (Cmax), AUC) with cardiac safety (ECG) data.Translational Strategy: Transformed complex laboratory measurements into actionable clinical insights for early-phase metabolic and cardiovascular research.Global Data Integrity: Ensured high-level data compliance and biostatistical consistency for multi-region submissions across Asian and European markets.
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Education
- Doctor of Medicine - MD, completed Residency Training in Internal MedicineIloilo Doctors' College of Medicine2004Rank 6 in medical graduating class, diplomate and fellow in internal medicine
- Bachelor of Science in Medical Technology (Medical Laboratory Science)University of San Agustin2000Licensed medical technologist, board topnotcher
Certifications
- EF SET (Rated with C2 English)Common European Framework of Reference (CEFR)2025
- Professional Certificate in Digital MarketingiMarketer London2018
Skill set
Categories
- Other