שרה אלבז -סי אר סי ייעוץ ומחקר קליני בע"מ

handling regulatory affairs, on-site monitoring of clinical trials, including , some project management; tracking enrollment rates, review and SDV of CRFs - all activities according to ICH-GCP guidelines, Sponsor's/CRO's SOPs and regulatory authorities requirements; preparation of scientific documents (i.e. clinical reports); provision of technical guidance and logistic services (drug importation, storage, distribution, etc.); problem solving; training and guidance of investigational staff and colleagues on basic monitoring; participation and presentation at investigator and other scientific meetings

וואטסאפ	sms	אימייל
פייסבוק	טוויטר	לינקדאין
https://www.veritiv.co.il/Code/Providers/Card.aspx?ProviderID=8258 העתק כתובת כרטיס