Experience

Siberian State Medical University

• Russian Federation
• Medical Practices
• 100 - 200 Employee

• • Jun 2021 - Present

• • Dec 2017 - Present

• • 2006 - Present

  Phase II - 6 trials, Phase III - 12 trials, Phase IV - 6 trials.Nosology: allergy and immunology, bronchial asthma, COPD, therapy.

• • Jan 2018 - Jun 2021

• • Nov 2014 - Dec 2017

• • 2014 - Nov 2017

  Deliver lectures, seminars. Guide, lead and mentor team in research projects. Maintain and develop research programs of Department. Prepare articles for publications, identify and obtain funds for research programs. Support grant writing and submission activities.

• • 2012 - 2014

  Deliver lectures, seminars. Assess, review and evaluate student activities and progress. Serve and support functional activities of departmental committees.

• • 2011 - 2012

  Department acting as SMO (Site Management Organization) and providing clinical trial related services. Created network of principal investigators. Developed a database of principal investigators, clinical trials, abilities of different facilities that includes their specialties, patient populations and their willingness to serve as clinical sites. Developed educational certification program «Good clinical practice for investigators» (ICH GCP).

• • 2010 - 2012

  Deliver lectures, seminars. Assess, review and evaluate student activities and progress. Serve and support functional activities of departmental committees.



European Respiratory Society

• Switzerland
• Non-profit Organizations
• 1 - 100 Employee

• Member

  • 2011 - Present



Sciencefiles

• Russian Federation
• Pharmaceutical Manufacturing
• 1 - 100 Employee

• Medical Writer

  • Jan 2013 - Jun 2014

  Produce regulatory documents related to the approval of pharmaceutical and medical products in liaison with government regulation agencies. Design medical texts (articles, reviews, materials for physicians and patients). Perform quality control of research projects. Compose documents that are suited for the intended audience of the publication, using accepted and standardized writing styles. Produce regulatory documents related to the approval of pharmaceutical and medical products in liaison with government regulation agencies. Design medical texts (articles, reviews, materials for physicians and patients). Perform quality control of research projects. Compose documents that are suited for the intended audience of the publication, using accepted and standardized writing styles.