

Clinical Pharmacologist with on-the-ground experience in oncology and HIV care, supporting physicians by delivering timely, evidence-based updates on treatment protocols and new therapeutic options. At a 900-bed oncology hospital, managed medication regimens, maintained up-to-date knowledge of chemotherapy protocols, and coordinated with pharmacies to ensure uninterrupted drug supply. At the HIV center, oversaw formulary development, conducted drug–drug interaction reviews across complex regimens (HIV, antibacterial, antiviral, and oncology therapies), and performed pharmacoanalytic assessments of bacterial flora and resistance patterns. Delivered regular physician education sessions summarizing current research and practical clinical applications. Strong ability to gather, interpret, and communicate clinical data, functioning as a bridge between research findings and real-world patient management.
1) Providing drug therapy recommendations to healthcare providers to ensure safe and effective use of medications:
2) Developing and implementing hospital-wide policies and procedures related to drug therapy:
3) Developing a standard for reporting adverse events through the automated information system "Roszdravnadzor"
4) Educating healthcare providers, patients, and caregivers on safe and appropriate use of medications by delivering lectures and conducting seminars on the topics:
5) Conducting pharmacokinetic consultations and therapeutic drug monitoring for patients with complex medical conditions or receiving high-risk medications.
6) Collaborating with other healthcare professionals to develop and implement comprehensive patient care plans.
The main responsibility during my career in Oncology Center named after N.P. Napalkov was ensuring the availability and timely receipt of all necessary chemotherapy drugs to meet the needs of the hospital's patients.
To fulfill this task, I utilized various methods for collecting data on the number of patients undergoing chemotherapy, their prescribed treatment regimens, the average and individual doses of medications, and the rate of their consumption. I then used this data to calculate the hospital's need for medications and to assess the budgetary expenditures associated with these drugs.
To ensure the accuracy of this data, I collaborated with the technical support center responsible for the hospital's information system's performance, the hospital's analytical department responsible for collecting statistical data, and the hospital's pharmacy responsible for receiving medications from suppliers and dispensing them to chemotherapy departments.
Also I was responsible for drafting preliminary responses to official letters from the Ministry of Health and sending final versions after approval by the chief.
In addition, I was included in clinical trials ongoing in hospital as a data-manager.
As a registered nurse I was participating in clinical trials in phase of bio-equality of researched medication compared to drug of choice. It included collection of blood samples for pharmacokinetic analysis of the investigational drug in strict accordance with the study design schedule, centrifugation and processing of biological specimens for further shipment to the research laboratory.