Trial Disclosure Specialist (EMA CTIS/CT.gov)
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Regulatory Affairs Professional | Bridging Pharma Transparency & Nutraceutical Innovation
I specialize in navigating complex regulations with precision, focusing on two key areas:
Expert in post-trial disclosures for EMA CTIS, ClinicalTrials.gov, and GCP compliance
Streamline processes to ensure timely, audit-ready submissions
Develop EFSA/FDA-compliant dossiers for health claims and product approvals
Combine scientific rigor with market-aware positioning
Why work with me?
✔ Dual Expertise: Unique perspective from working across pharma and nutraceuticals
✔ Agile Problem-Solving: Leverage AI tools and strategic thinking to simplify compliance
✔ Holistic Communication: 10+ years in wellness coaching enhances stakeholder collaboration
Passionate about making regulations work for business goals — not against them.
