Seasoned 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 23 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. Knowledgeable and adept at recognizing clinical values and abstract data from source documents. Uses analytical skills to identify data or patient safety issues. Enthusiastic and eager to contribute to team success through hard work, attention to detail and excellent organizational skills. Motivated to learn, grow and excel. Excellent reputation for resolving problems and improving patient satisfaction. Recognized consistently for performance excellence and contributions to success. Strengths are organization, multi tasking, communication with the doctors and companies and deadline driven.
I work with a company Targeted Medical Education and do the IRB submission for all the PI's across the US.
I also have a contract with a Breast Surgeon in CA and do his research home based.
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