Radim Geryk

Project Manager Of Preclinical Studies at QUINTA-ANALYTICA

Radim Geryk has a diverse work experience. Radim worked at Quinta Analytica from 2016, where they served as the Validation Team Head, responsible for developing and validating bioanalytical methods for active substances in biological samples. Radim was also the Responsible Analyst for the analytical part of bioequivalence studies. From 2016 to 2018, they worked as an HPLC/MS/MS analyst at Quinta Analytica as well.

In 2020, Radim Geryk worked as a high school chemistry teacher and science popularizer at Gymnázium.

Radim has also worked as a Junior Research Scientist at the Karl-Franzens-Universität Graz, Institute of Pharmaceutical Sciences, and the Charles University in Prague. Additionally, they worked as a Quality Controller at Heaven Labs s.r.o. - MANA and as a Junior Research Scientist at the RCPTM - Regional Centre of Advanced Technologies and Materials.

Radim Geryk has a strong educational background in Chemistry and Physical Chemistry. Radim obtained a Master's degree in Chemistry from Charles University from the year 2010 to 2012. Following this, they participated in a lifelong learning program at Charles University from the year 2012 to 2014, specializing in Chemistry. Additionally, they earned a Research Doctorate in Physical Chemistry from Charles University between the years 2012 and 2016.

In terms of certifications, Radim Geryk obtained the "First Certificate in English" from Cambridge English Language Assessment in March 2015. Radim also completed a course on teaching chemistry for secondary schools, titled "kurz Celoživotního vzdělávání - učitelství chemie pro střední školy," at Univerzita Karlova v Praze in July 2014.

Location

Prague, Czech Republic

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QUINTA-ANALYTICA

Quinta is a GCP/GLP/GMP-certified, EMA and FDA-inspected European CRO offering in-house clinical testing, pharmaceutical analysis, CMC and R&D. Quinta specializes in clinical studies, bioanalytics, method development and quality control for both small and large molecules, human and veterinary IMPs as well as generics. We provide unrivaled expertise to worldwide pharmaceutical and biotechnological clients across the entire pharma spectrum. Quinta is part of the Conscio group with headquarters in Munich, Germany, laboratories in Czechia, Austria, Slovakia, Germany and offices in the USA. Our main service areas include: 1) Clinical Testing: With 2 in-house clinical units providing BE/BA/PK studies, with capacity for 60+40 beds. 2) Bioanalytical Testing: GLP/GCP solutions for preclinical & clinical studies, small & large molecules, BE/BA/PK. 3) Research & Development: Analytical R&D, impurities, extractables & leachables, degradation, trace studies. 4) Pharmaceutical Quality Control: GMP quality control, batch testing, stabilities, HAPIs, inhalation, API sourcing. 5) Microbiology: GMP sterile & non-sterile testing, microbial/water analyses, endotoxins, antibiotics & vitamins. 6) Biopharmaceutical Quality Control: GLP/GMP bioanalysis, CMC, characterizations of peptide & protein IMPs, biosimilars. Quinta was founded in 1997 and has been successfully inspected by FDA more than 10 times. Quinta is headquartered in Prague, Czech Republic.


Employees

51-200

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