Technicien d'études cliniques H/F - CDD 3 mois – temps plein
Based in France
Core
Participate in simple technical clinical studies, manage study documents, control data entry quality, and assist in monitoring visit preparation.
Role type
Clinical Study Technician
Builds
Clinical studies for pharmaceutical, food, and environmental industries
Domain
Clinical research / Life sciences
Required skills
Data entry, document management, quality control, regulatory knowledge (preferred), adaptability
Preferred skills
Knowledge of clinical trial regulations, prior experience as a Clinical Study Technician
Technologies
None stated
Responsibilities
Participate in clinical studies, manage study documents, control data quality, prepare for monitoring visits
Seniority
Junior, entry-level