PARIS
Clinical/Regulatory Affairs Consultant with significant experience in the medical device and pharmaceutical industries, including pulmonary, cardiovascular, oncology and ophthalmic products. Scientific background with proven expertise in developing clinical trial strategy, design, and implementation, supporting clinical trials, Ethics and Competent Authority submissions and interacting with international agencies.
Mes compétences :
Affaires réglementaires
GCP/BPC
Recherche médicale clinique
Dispositifs médicaux
