I have quite a rich history in the pharmaceutical industry, demonstrating expertise in regulatory submissions, compliance, and pharmaceutical law. I started at the laboratory of pharmaceutical development, continued as a project manager and after joined clinical trials. I am proficient in managing global complex projects and collaborating with multiple stakeholders to ensure regulatory compliance and drive product approvals. With a strong scientific background, I am capable to navigate the regulatory landscape and align business objectives with regulatory requirements.
I fluently speak 5 languages: English, German, Polish, Ukrainian, Russian.
Besides my accomplishments in the pharmaceutical industry, I have also spent several years teaching English and German. This experience has significantly enhanced my soft skills and ability to communicate effectively.More...