A motivated, dedicated senior Clinical Research Assistant
Clinical research is a highly regulated, time-consuming field: this is why partnering with a clinical research assistant is a good way to better optimize and oversee your clinical research activity – in compliance with GCP/ICH.
With a significant experience in national and international studies, mainly in oncology (early phases, phase III studies) and kidney transplantation (phase IV study), but also in epilepsy, infectious diseases, ophtalmology and ICU, I will be your best asset!
English/French speaker
Bordeaux area (France)
My professional skills
Data entry, reports
& queries
- CTMS entries
- Site visit reports (SVR)
- Monitoring/Entry of clinical data
- Queries management
Site initiation and monitoring
- Preparation/conduct of site visits
- TMF management
- Optimizing patient recruitment
Team coordination and management
- Coordination of involved staff
- Privileged contact with sponsor
- Overview of Quality
Activities
communication
- WordPress website management
- Newsletters drafting
- Facilitating meetings
About me
As a Clinical Research Associate based in Bordeaux area, I have gained experience in public institutions (Pasteur Institute, Unicancer…) and international CROs.
Mobile within the south-west region of France, I have been involved in large-scale projects, managed dozens of sites and trained in several therapeutic areas.
