Freelancer profile translated to English.

Description

Clinical research technician with 2 years of experience at the CHU de Rennes, I offer my services as an independent clinical research assistant.

With 28 years of experience as a laboratory technician, I have developed strong scientific rigor and excellent knowledge of the hospital environment, which I now bring to clinical research.

I provide support to clinical and data teams in the management and quality of clinical trial data, in compliance with Good Clinical Practices (GCP).

Key Skills:

Data entry and validation in eCRFs

Data cleaning and query management

Patient data consistency checks

Document management (ISF, TMF)

Protocol monitoring and regulatory compliance

My Approach:

Rigorous, organized, and autonomous, I quickly integrate into existing teams and tools. I pay particular attention to data quality and compliance with regulatory requirements.

Terms:

Available for ad-hoc or regular assignments

Remote or on-site work

Adaptability to tools and environments (eCRF, clinical software)

📩 Feel free to contact me to discuss your needs.

Industry field of expertise

Languages

French
Native or bilingual

Workplace preferences

Can work on-site

Paris (up to 20km)

CHU DE RENNES
CLINICAL RESEARCH TECHNICIAN
MEDICAL
January 2020 - July 2022 (2 years and 6 months)
Rennes, France
Participation in the management of clinical studies within a university hospital center.

Main tasks:

- Data entry and validation in eCRFs
- Data cleaning and query management
- Verification of patient data consistency
- Protocol monitoring and compliance with Good Clinical Practices (GCP)
- Management and updating of study documents (ISF, patient files)
- Collaboration with CRAs and medical teams
eCRF Data cleaning / query management Documentation management Data Management Protocol management
CHU DE RENNES
LABORATORY TECHNICIAN
MEDICAL
July 1992 - January 2020 (27 years and 6 months)
Rennes, France
- Performing and checking tests and analyses according to established protocols
- Verification, organization, and validation of experimental results
- Management and monitoring of documentation and technical files
- Strict adherence to quality procedures and regulatory standards
- Training and support of new employees on best practices

This experience allowed me to develop essential skills in organization, precision, and adherence to regulatory standards, skills directly transferable to data management and clinical study monitoring.
Protocol management Documentation Management Regulatory Compliance Data Quality
CERBALLIANCE
LABORATORY TECHNICIAN
MEDICAL
May 2023 - Today (3 years and 1 month)
Saint-Grégoire, France
- Performing and checking tests and analyses according to established protocols
- Verification, organization, and validation of experimental results
- Management and monitoring of documentation and technical files
- Strict adherence to quality procedures and regulatory standards
- Training and support of new employees on best practices

This experience allowed me to develop essential skills in organization, precision, and adherence to regulatory standards, skills directly transferable to data management and clinical study monitoring.
Protocol management Regulatory Compliance Data Quality Documentation Management