Description
PROFESSIONAL SUMMARY Persistent, Organized and detailed oriented professional interested to pursue a position as a Clinical Research Associate (CRA) with a pharmaceutical / biotechnology firm where I can utilize my medical and clinical research knowledge along with my strong technical and procedural skills in clinical monitoring to meet the growing needs for clinical trials of new drugs in multiple therapeutic areas. CORE QUALIFICATIONS * Result oriented, problem solver with the ability to perform 3-5 site visits/week * Detailed Oriented * Hard working individual with the ability to travel 60 -70% * Quick learner with great knowledge of GCP guidelines. * 2+ years of experience monitoring Phase II/III clinical trials * Knowledgeable in use of EDC, I-track, Trackwise, Medidata, InForm, CTMS, eClinical * Excellent Oral and Written Communication skills
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