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Freelance Researcher & Transcriptionist
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email@example.com • 310-739-3058
Clinical research professional with extensive knowledge of clinical trial operations and web-based data collection systems. Experience includes study coordinating both NIH and drug sponsored, longitudinal/short-term trials, wet-bench lab technique, data collection/management, patient recruitment/retention skills and obtaining patient consent/administering HIPAA. Sound familiarity with clinical study monitoring, medical terminology, FDA, ICH and GCP regulations. Strong ability to work and communicate with medical professionals. Highly ambitious, with excellent interpersonal and communications skills. Extremely organized and detail-oriented.
08/2010 – 04/2011 Clinical Research
Oceanside, California, United States
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