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 שם איש קשר:
