Detail oriented clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Certified in Good Clinical Practice. Skilled at collecting specimens, dispensing medications during the course of clinical research trials. Experienced in coordinating schedules, results and documentation. Knowledgeable in ICH GCP and adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues.
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