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.

Industry field of expertise

Languages

English
Native or bilingual

Workplace preferences

Remote only

Primarily works remotely

Icon clinical research
Clinical Research Associate
HEALTH AND WELLNESS
August 2025 - Today (10 months)
Mechelen, Belgium
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
HEALTH AND WELLNESS
December 2023 - April 2025 (1 year and 4 months)
Ghent, Belgium
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