Anna Kurbatova
- مكان العمل: أوكرانيا, كييف, Bioage / BioAge (Mediland Stem Cell Therapy Center)
- European Director of Clinical Trials at the clinic, overseeing European operational activities across clinical sites, laboratories, and biobanking facilities.
- Manages planning, implementation, and monitoring of clinical trials with EU regulatory compliance covering EMA, GCP, and GDPR.
- Supervises site selection, investigator coordination, and cross-border logistics for clinical studies, including support for regulatory submissions, audits, and inspections.
Anna Kurbatova is a specialist at the clinic and the clinic’s European Director of Clinical Trials. She coordinates European trial operations across sites, laboratories, and biobanking facilities, with EU compliance covering EMA, GCP, and GDPR. For international patients, her role is central to ensuring trials are executed with clear operational alignment between research, clinical, and manufacturing teams.
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المؤهلات العلمية
Clinical trials run on details that patients never see—site readiness, documentation, and regulatory alignment. At the clinic, Anna Kurbatova works as European Director of Clinical Trials, coordinating operational activities across clinical sites, laboratories, and biobanking facilities. Her work covers trial planning, implementation, and monitoring under EU regulatory requirements, including EMA, GCP, and GDPR. She also supports cross-border logistics and investigator coordination so studies can move forward without avoidable delays.
For patients traveling internationally for stem cell–related programs, this operational layer matters: it helps ensure ethical standards, patient safety protocols, and the regulatory approvals needed for trial execution are handled systematically. Kurbatova’s responsibilities also include optimizing workflows to improve efficiency, quality, and trial timelines. She collaborates with academic institutions, CROs, and healthcare partners to keep research, clinical, and manufacturing teams aligned during execution.
Education
Work experience
- European Director of Clinical Trials — Mediland Clinic (European operational oversight across clinical sites, laboratories, and biobanking facilities; planning, implementation, and monitoring of trials in compliance with EU regulatory requirements)
Clinical focus and techniques
Anna Kurbatova’s clinical-trial focus is operational rather than procedural—centered on ensuring trials are executed under EU standards and supported by biobanking and laboratory workflows.
- Clinical trial management with EU regulatory compliance: EMA, GCP, GDPR
- Biobanking operations to support clinical trial execution
- Site selection, investigator coordination, and cross-border logistics for clinical studies
Professional societies and certifications
Academic output
Courses and advanced training
Awards and recognition
Patients typically interact with the clinic’s medical team for consultations, while Kurbatova’s work supports the trial infrastructure behind the scenes. The clinic’s international pathway includes travel arrangements for patients who proceed with therapy in Ukraine, and trial execution depends on the same operational discipline across sites and laboratories.
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