Fereshteh Zarebidaki

• Medical terms in oncology trials. • Clinical trial Site management by acting as a communication point between sponsor and clinical trial site personnel. • Problem solving as proven by identifying deficiencies in conducting clinical trials and taking corrective and preventative actions. • Writing regular reports and follow-up letters. • Working with different vendors, such as ePROs, central lab, EDC, etc.

-Medical Writing and Medical Device • Clinical Evaluation Report, MEDDEV 2.7/1, MDR • Writing: study plan, synopsis, informed consent form -Clinical Data Management • CDISC (STDM implementation guide) • Edit checks • eCRF design and annotation • ICP-GCP Guidelines -Pharmacovigilance • MedDRA coding • Safety reporting and pharmacovigilance database

During my PhD in Charite Universitätsmedizin, I was working as research assistant in the laboratory. I have accomplished several collaborations which are published in top journals in the field.

During my PhD project I accomplished many national and international collaborative projects. I have explored the mechanism of synapse function.