Knowledgeable CRC adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues. Focused Clinical Research Coordinator well-versed in study protocols, standard operating procedures and general trial oversight. Excellent problem-solving abilities with a detail-oriented nature. Ready to bring 10-15 years of related experience to a challenging new role. Versatile 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. Skilled at collecting specimens, dispensing medications and consulting with patients during the course of clinical research trials. Experienced in coordinating schedules, results and documentation. Multi-talented CRC consistently rewarded for success in planning and operational improvements. Experience in policy development and staff management procedures positively impacting overall morale and productivity.
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