Description

I am a Clinical Research professional with hands-on experience supporting and monitoring clinical trials in compliance with ICH-GCP and EU regulations.

I have worked as a Clinical Trial Assistant and CRA, supporting study start-up, site management, essential documents, TMF/ISF review, monitoring activities, and site communication.

I am detail-oriented, well-organized, and experienced in working with sponsors, CROs, and investigational sites across different therapeutic areas. I support clinical teams with accuracy, regulatory compliance, and clear communication to ensure smooth trial execution.

Available for remote or hybrid assignments including CTA support, CRA support, TMF review, site start-up, and clinical documentation.

Domaines d’expertise

Langues

Anglais
Bilingue ou natif

Préférences en matière de lieu de travail

En télétravail uniquement

Travaille majoritairement à distance

Icon clinical research
Clinical Research Associate
SANTÉ & BIEN-ÊTRE
août 2025 - Aujourd'hui (10 mois)
Mechelen, Belgique
Responsible for site monitoring activities, site start-up support, and review of essential documents in compliance with ICH-GCP. Ensure data quality, accurate documentation, and effective collaboration with investigator sites and internal teams.
Sillar Clinical
Clinical Trial Administrator
SANTÉ & BIEN-ÊTRE
décembre 2023 - avril 2025 (1 an et 4 mois)
Ghent, Belgique
Detail-oriented Clinical Trial Assistant with experience supporting EU and global clinical studies in compliance with ICH-GCP, EU CTR, and ALCOA+. I provide reliable operational support to CRAs and study teams, including TMF/ISF maintenance, study start-up support, essential documents tracking, site coordination, and monitoring visit preparation/follow-up. Highly organized, proactive, and comfortable working independently or within CRO/sponsor teams.
Communication Organisation Time management Documentation management