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Nadiia Zubchuk


1 analyzing ICH, FDA, EMA guidelines to estimate the nonclinical studies requirements;
2+ analysing of scientific data in the field of non-clinical research;
1 normative-legal regulation on issues state registration of medicines;
1+ writing essays, research proposals, case studies in English for foreign
students with specialization in medical sciences and biology
7+ research work;
3+ biology tuition for pupils and medical students.


Preclinical trials specialist, YURiA-PHARM LLC. April 2021 – present
Conducting scientific literature research, reviewing scientific experiments and documentation to design plan of preclinical studies;
Organizing preclinical studies;
Supporting product development with scientific input and generating scientific documents to support the generation of registration documents;
Reporting, interpreting, and presenting scientific/technical results to management;
Acquiring and evaluating data that establish the biological safety of impurities in drug products and substances;
Analyzing ICH, FDA, EMA guidelines to estimate the set of nonclinical studies that have to be conducted to prove the safety, potency, and quality of human pharmaceuticals and vaccines


Ce profil vous semble pertinent, contactez Justin Merlin pour obtenir son CV complet et sa lettre de motivation : justine.merlin@lyonbiopole.com