The knowledgeable clinical research assistant is adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues. A versatile clinical research professional is 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 Taiwan. Skilled at collecting specimens, dispensing medications, and consulting with patients during the course of clinical research trials. Experienced in coordinating schedules, results, and documentation. 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 2.2 years of related experience to a challenging new role.