DeVona R.

Experienced Clinical Research, Data and Quality Management Professional with a demonstrated history of working in the biotechnology, laboratory, and clinical research industry and managing complex projects for Hematology & Oncology clinical trials. Skilled in EDC databases such as Redcap, Veeva Vault, Bioclinica/Clario, & MediData Rave. Proficient in the Code of Federal Regulations for Clinical Trials and Good Clinical Practices, Business Development, Quality Improvement, Leadership and Training. Strong clinical monitoring professional for Phase I-IV Trials with a MS Degree focused on Clinical Research Science and Product Development. AREAS OF EXPERTISE EDC Data Abstraction CFR/FDA Guidelines CTMS Data Management Oncology and Hematology Clinical Trials Good Clinical Practices Quality/Project Management Institutional Review Board Requirements Clinical Monitoring Regulatory Writing/Editing Quality Audits Research Billing Training Adverse Event Reporting Corrective Action Plans