Amgen Hematology-Oncology, Global Study Management. Oncology has been my primary therapeutic area of focus in research for the past nine years. I have extensive experience as a Clinical Research Associate and am currently expending my knowledge and skill set on the project management side as a Sr. Associate in Global Study Management.
Sr. Clinical Trial Specialist @ Responsible
Amgen Hematology-Oncology, Global Study Management. Oncology has been my primary therapeutic area of focus in research for the past nine years. I have extensive experience as a Clinical Research Associate and am currently expending my knowledge and skill set on the project management side as a Sr. Associate in Global Study Management.
Sr. Clinical Trial Specialist @ Responsible for the conduct of a clinical trial at the regional or global level including maintaining the study budget and data timelines, ensuring adequate resources as well as the development of clinical documents. Assist in the training and mentoring of Clinical Trial Managers. From June 2011 to Present (4 years 6 months) Clinical Research Associate @ From 2001 to 2003 (2 years)
Mira Polovina is skilled in: Pharmaceutical Industry, Clinical Trials, CTMS, GCP, CRO, Clinical Monitoring, ICH-GCP, Clinical Research, Oncology, Clinical Development, Infectious Diseases, Therapeutic Areas, Clinical Data Management, SOP
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