Bosilka is experienced Regulatory Affairs Specialist with a demonstrated history of working in the wholesale industry. Skilled in Regulatory Affairs, Pharmacovigilance, Clinical Trials and strong legal professional background with a Master’s Degree focused in EU Regulation.
She has gained her six-year Regulatory experience supporting and acting as Regulatory Affairs Associate and QPPV for respective Pharma companies such as Pfizer, Mylan, Berlin Chemie, Octapharma and many more.
Currently, she is working as a Senior Specialist Regulatory Affairs in PharmaLex Bulgaria and mainly supporting as global point for regulatory matter per Bayer CH project.
Her dissertation in Pharmacovigilance and managing safety data in Clinical trials also led her to sustainable experience in Clinical trials and international differences in regulations on SUSARs.
