sub-investigator Company NameASCENT CRS Moscow, Russian Federation Key responsibilities: • All procedures during clinical part of the trial according to trial protocol and SOPs • Training of nursing staff, • Communication with sponsors • Conducting the bioequivalence, I, III and IV phase trials (anti-inflammatory drugs, nephrology, gematology, neurology, cardiology, hepatology, oncology, endocrinology, allergology) • Working with and review of study documentation as CRF, ICF, Protocols, IB • Providing scientific background on the project manager requests • Medical monitoring. Clinical Research Associate Company NameAbbVie Moscow, Russian Federation
Pulmonology