Katarzyna Misiura

- Monitoring and coordinating of the clinical trials conducted by the Company
- Establishing and maintaining contacts with the clinical centers, researchers and/or external experts
- Preparing and reviewing documentation necessary to register a clinical trial in accordance with the requirements of Good Clinical Practice and applicable regulations;
- Checking the completeness and quality of clinical trial reports, coordinating the process of documentation additions to the comments made by the Registration Offices;
- Cooperation with other departments of the Company to ensure timely conduct of the study design;
- Design and analysis of the assumptions for new clinical trials phases I-IV and bioequivalence.

- Coordinating project activities associated with functions of clinical research studies.
- Responsibility for clinical trials initiation visit within the company.
- Providing accurate, timely, and consistent study information to both sponsors and internal departments to support business needs.
- Managing the project and adapting to Good Clinical Practices and relevant regulations. Coordinating medical trials and new projects within the company.
- Data review and source data verification
- Contact with clients and monitors,
- Report Serious Adverse Event (SAE), (AE).
- Coordinating clinical data in CRF, generating and resolving query.
- Management of clinical trial activities to ensure the integrity and compatibility of clinical data with GCP and source documentation.

Przeprowadzanie auditów. Doradztwo dla firm w dziedzinach związanych z jakością i Systemami zarządzania jakością. Prowadzenie szkoleń z tematyki ISO 9001-2000; ISO 14001-2004.

Prowadzenie terapii odczulających metodą biorezonansu
Wykonywanie testów alergicznych
Prowadzenie gabinetów medycznych w różnych lokalizacjach
Kontakt z pacjentem, opracowywanie strategii marketingowych.

Praca w laboratorium fizykochemicznym, oczyszczalni ścieków, mikrobiologicznym
Interpretacja wyników pomiarów do nadzoru procesów technologicznych