Sonya Gaudioz

With 15 years of experience in clinical research, particularly in oncology, I support research centers and sponsors in the implementation, monitoring, and success of their clinical studies. As an independent consultant, based in the Rhône region, I work throughout France for positions as a Clinical Research Associate (CRA) or Clinical Trial Technician (CTA).

Expertise and know-how:

Complete clinical study management: site selection and initiation, monitoring, data tracking, site closure. Management of phase I to IV trials, observational studies.

Regulatory mastery and compliance: application of Good Clinical Practices (GCP), compliance with French and European legal requirements, regulatory submissions and management of audits and inspections.

Data analysis and management: data collection and validation (CRF/eCRF), query resolution, quality control, and deadline adherence.

Support for investigator teams: operational management, training, protocol awareness, and personalized follow-up to ensure study success.

Why collaborate with me?

Adaptability and mobility: Available for assignments throughout France, with a great capacity to quickly integrate into your teams.

Commitment and professionalism: Results-oriented, I make it a point of honor to meet deadlines, objectives, and quality standards.

Do you have a clinical research project or mission? Contact me to discuss your needs and explore the solutions I can offer.