Clinical Research Associate

I am a Clinical Research Associate with experience in paediatric clinical investigation, clinical operations, and regulatory compliance. I manage clinical trial activities from start-up and site activation through conduct, close-out, and archiving.

I have supported studies across obesity, metabolic, rare disease, liver, and thyroid therapeutic areas.
My work includes sponsor and CRO collaboration, investigator communication, monitoring visit preparation, data cleaning, source data verification support, SAE follow-up, eCRF review, and query resolution.

I bring strong knowledge of Good Clinical Practice, data integrity, regulatory documentation, and trial systems. I am trained in ICH-GCP R3 and experienced with EDC, IRT, and eTMF platforms including Medidata Rave, REDCap, Veeva Vault, and Ennov.

Before moving into clinical research, I worked as an osteopath, senior clinical professor, and research supervisor. I developed training programmes, supervised student research and methodology projects, and worked within multidisciplinary oncology care teams.

I am fluent in English and a native French speaker. I combine clinical knowledge, strong organisational skills, problem-solving, stakeholder management, and a commitment to high-quality, compliant clinical research.