Since November 2015
•Identify, develop and maintain collaborative relationships with current and future external thought leaders and key regional healthcare professionals (HCPs) • Respond to HCP requests for clinical / scientific information • Work with IIT Manager to co-ordinate proposals around Investigator Initiated Trials (IITs) • Delivery of scientific training to internal colleagues • The provision of medical insight to relevant Celgene colleagues
Compliance Oversight Lead
May 2015 --- November 2015
Local oversight of assigned clinical trials to ensure patient safety and quality study execution in accordance with prevailing laws, Good Clinical Practices, and company standards. •Ensure overall quality and regulatory and GCP compliance. •Perform protocol specific quality review visits . •Attend Investigator meeting/protocol training to ensure clear understanding of the protocol requirements. •Support local Investigator relationship management. •Support Audit/inspection for assigned project when appropriate and follow through audit/inspection finding resolution.
March 2013 --- May 2015
Medical and scientific support in a cross-functional team • Taking part in development and achievement of strategy, tactics, and operating plan advancing the marketing of Company products • Providing scientific support and expertise to cross-functional team and other internal stakeholders with respect to promotional materials creation process, advertising and educational programmes, clinical research, medical information, regulatory issues in compliance of ethical business principles. • Providing educational support inside cross-functional team as well as Field Force training in appropriate therapy area medical knowledge Medical and scientific support to key external stakeholders and develop professional skills: • Establish peer-to-peer relationships with Key Medical Opinion Leaders (KOL), scientists, clinical and research leaders, institutions and centers in the country to foster Pfizer's efforts to establish and maintain its therapeutic leadership position
Clinical Research Associate (CRA)
June 2008 --- March 2013
Participate in the creation of clinical trial documents in collaboration with the clinical project leader. * Identify and select investigators in collaboration with the clinical project leader * Prepare / collect all documents needed prior to study initiation. * Perform / participate in study set up visits in the investigational centres and organises / participates in study initiation meetings in which are provided scientific and technical knowledge concerning the study procedures and its organisation. * Follow up of trial progress and quality control of data (source document check). * Documentation of protocol violations, adverse events and premature treatment cessation. * Identification and resolution of all problems: logistical, methodological, human technical, which occur during a study. *Management of the local trial files *Management of the investigator’s trial file * Detection and reporting of deviations, finding and implementing corrective measures * Provide timely written documentation of all visits / contacts in appropriate reports.
April 2007 --- May 2008
Prevention and treatment of eye's disiases, incl. both theraputic and surgery approaches.
October 2006 --- May 2008
Prevention and cure eye's disorders in Optometry.
September 2004 --- September 2005
Prevention and cure of eye's diseases with mainly therapeuteic focusing.
Doctor of Medicine (MD) in Residency in Ophthalmology from Russian State Medical Academy of Aftergraduate Education in 2005
in Teaching English as a Second or Foreign Language in the Medical area from Tver State University in 2003
Doctor of Medicine (MD) in General Practice from Tver State Medical Academy in 2003