Attaché de Recherche Clinique Biopharma (H/F)
Core
Monitor international clinical studies ensuring protocol, regulatory, and timeline compliance while representing AstraZeneca's ethics to investigators.
Role type
Clinical Research Associate (CRA)
Builds
Clinical study execution and data management
Domain
Biopharma / Clinical Trials
Deliverable
client delivery
Required skills
Clinical trial methodology, Good Clinical Practice (GCP), pharmaceutical regulations, data management, document management, study monitoring
Preferred skills
Scientific degree (Bac +5), specific ARC training (DIU FARC or equivalent), 3+ years pharma industry experience, driver's license B, computer tools proficiency, English (intermediate)
Responsibilities
Prepare, set up, follow, close, and control international clinical studies; manage data and documents; ensure regulatory and protocol compliance; represent company ethics to investigators.
Seniority
Mid-level, hands-on IC