Blaho Bogumiła
Clinical Research Associate
Wesley C Van?Voorhis
Poland
Biography
"Key duties: - Monitor the conduct of clinical trials, especially enrolment and quality of data in Phase III Trials (area of Cardiology, Diabetology)  - Verify subject safety and site adherence to HA and ECs Regulations (for Poland and Czech republic), and ICH/GCP Guidelines.  - Review CRF, Informed Consent Documents - Ensure complete and thorough study drug reconciliation.  - Manage trip reports, letters, query resolutions and expenses.  - Manage site master file contents and work with sites to ensure communication requirements between site and IRB are adhered to. - Provide support and timely follow-up for all audit and quality assurance activities.  - Instruct sites in the use and maintenance of an IVRS device.  - Prepare submissions of study related documents to ECs in Czech rep. - Conduct of trainings/presentations at Local Investigators Meeting in Czech republic. UW Degree Name Master's degree Field Of Study Języji specjalistyczne - Tłumaczenia (Eng.) Dates attended or expected graduation 2008 – 2013 Akademia Podlaska w Siedlcach Akademia Podlaska w Siedlcach Degree Name Master's degree Field Of Study Biologia, ogólni"
Research Interest
clinical research
