Personal Information
Organization / Workplace
Greater Nashville Area, TN, TN United States
Occupation
Clinical Research Associate II at Sarah Cannon Research Institute, Development Innovations
Industry
Medical / Health Care / Pharmaceuticals
About
• 4 years of CRA experience (2 years home-based/travelling; 2 years in-house/central) monitoring Phases I, II, and III clinical trials in oncology therapeutic area (i.e. carcinoma, sarcoma, lymphoma, and leukemia) across 50+ research sites nationwide; adhering to FDA regulations and ICH-GCP guidelines; and utilizing disease assessment response criteria (e.g. RECIST, Cheson, Hallek, RANO).
• 3 years of laboratory, biomedical and pre-clinical research experience.
• Proficient and adaptable to all Electronic Data Capture and Clinical Trials Management Systems, with experience in Medidata CTMS and Rave, OmmniComm TrialMaster EDC, and Oracle’s Siebel CTMS; and skilled with Microsoft Office pro...
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