Majda has ten years of experience in phase I-IV clinical trials and post-marketing pharmacovigilance, including various therapeutic areas and medicinal products. Areas of expertise include case processing, safety reporting, development of PV controlled documents (such as standard operating procedures, operating guidelines, safety management plans, etc), active participation and support in regulatory inspections and audits and project management.
Majda is fluent in several European languages.
Majda is based in Belgrade, Serbia.