MDU has highly qualified, experienced and effective team of Clinical Research professionals.

We have experience in all areas of Clinical research including feasibility, Project management, Start-up, insurance, quality assurance and Monitoring.

 

Our Team:

Anton Terentyev MD is a Certified Clinical Research Professional with 10 years of extensive International Project Management, Leadership and Monitoring experience in all therapeutic areas. Qualified as Internal Medicine Doctor.

Involved in Clinical Trials since 2007 year. Anton was the first employee of AstraZeneca Ukraine Clinical Research department. Has experience in office Start-up including managing the operational aspects of projects to meet contractual requirements in accordance with SOPs, policies and practices.

Performed over 30 Phase II and III Clinical Trials in all Therapeutic Areas. Has Experience of Regional Therapeutic Area Specialist in Pulmonology.

Was on position of Regional Clinical Project Manager Regional department Central-Eastern Europe and Meddle East-Africa.

Has letter of appreciation from President of AstraZeneca.

 

Viktor Zaviriukha MD is a Certified Clinical Research Professional with 5 years of International Monitoring and Project Management experience. As a Clinical Project Manager Viktor Zaviriukha as a core project team member representing clinical delivery with the customer.

Qualified as gynecology doctor.

In previous roles, Viktor Zaviriukha has managed and monitored phase III, IIIb, IV, observational/non-interventional, and Registry studies, and is experienced in the following therapeutic areas: Cardiology/CVD, Endocrinology, Infections & Infectious Disease, Nephrology, Neurology, and Oncology (NSCLC).  Viktor Zaviriukha has participated in several Sponsor and Investigator`s Meetings worldwide (EU) and has experience with site, eTMF and financial audits, as well as review and resolution of CAPAs.

As the result of 2 years project manager work – 2 successful delivering of projects in oncology and internal medicine areas. He successfully passed independent audits and EMEA inspection.

 

Anna Sanina is a Senior Clinical Research Associate with 5 years of Monitoring experience. Qualified as biologist in immunology. MSc

Started to work as a CRA since 01 November 2012.

Was promoted to the Sr. CRA position since 01 Apr 2015.

Has good experience in the scientific research programs, worked in the clinical hospital, in the different types of laboratories, including recent technologies. Took part in scientific research (immunology), has worked in the field of diagnostics of child’s oncohematology since 2009.

As CRA Anna took part in 16 Phase II and III Clinical Trials in Endocrinology, Cardiology, Gastroenterology and Nephrology with exceptional quality and number of appreciations.

Anna is experienced with all main eCRFs and IXRS systems.

 

Sergii Palkovskyi MD is a Senior Clinical Research Associate with 8 years of Monitoring experience. Qualified as Pulmonology doctor.

Sergii Palkovskyi MD Started his career in clinical trials as investigator in Ukraine Research Institute of Pulmonology. As Investigator Sergii took part in 9 Clinical trials.

Started to work as a CRA since May 2012.

Was promoted to the Sr. CRA position since 15 Sep 2014.

As CRA Sergii took part in 18 Phase 2 and 3 Clinical Trials in Pulmonology, Endocrinology, Cardiology, Gastroenterology and Neurology with exceptional quality and number of appreciations. Sergii is experienced with all main eCRFs and IXRS systems.

 

Oleksandr Terentiev MD. Medical affairs Manager and Qualified Person Responsible for Pharmacovigilance since 1998.

Started his career in Medical Affairs after being retired from Military Medical Service as a Colonel. Qualified as Internal Medicine doctor.

Full medical support in development and update of operating procedures according to changes of requirements of global procedures and requirements local Authorities organizations. Interaction and exchange of PVG information with the local Authorities organizations and Marketing authorization holders.

Full submission/approval and RA maintenance of 13 clinical trials. Took part in audits and inspections which conducted by the Authorities organizations and audits conducted by Marketing authorization holders.