Cromos Pharma
Tatiana Chasovskaya is an experienced project manager specializing in clinical trials and regulatory affairs, currently serving as a Project Manager at Cromos Pharma since February 2022. Prior experience includes the role of Clinical Research Project Manager at Gedeon Richter Plc. from July 2015 to February 2022, overseeing project management in clinical trials and regulatory affairs. Earlier, Tatiana worked as a Project Manager at ChemDiv, Inc. from June 2013 to July 2015, where responsibilities included strategic planning and technology transfer coordination. Tatiana began their career as a Research Scientist at the Emanuel Institute of Biochemical Physics, Russian Academy of Sciences, focusing on cell membrane transport and antioxidants. Academically, Tatiana holds a Master of Science in Pharmaceutical Medicine from Hibernia College, a PhD in Biology from the Institute of Biochemical Physics, and multiple degrees in Biochemistry and Applied Science from the Moscow Institute of Physics and Technology.
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Cromos Pharma
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Cromos Pharma is a US-based, international contract research organization delivering fully integrated clinical research solutions, in all trial phases, across a wide range of therapeutic indications. Our expert team, comprised of 95% MDs, has extensive expertise in study design, medical writing, regulatory affairs, site management, patient recruitment and data management. Cromos Pharma has experience in delivering success in a wide range of trial types, from biosimilars and generics, to successfully managing trials of novel therapeutics in a wide range of clinical indications. Our team provides full-service solutions to international pharma and biotech companies in high-recruiting regions, assuring exceptional data quality. Cromos Pharma combines global expertise with in-depth experience and knowledge in the US, Central and Eastern Europe, Central Asia, Republic of Georgia, and Türkiye resulting in rapid patient recruitment. Our team has met or reduced enrollment timelines in 95% of conducted trials. We provide accelerated study start-up timelines in our regions of operation. Regulatory inspections by FDA and EMA and site audits attest to the highest quality of our clinical data. Established in 2004, Cromos Pharma has strong regional experience that is supported by a global network of offices. Its international HQ is in Portland, Oregon, USA and its European HQ is in Dublin, Ireland.