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Susan Parker

Quality Management

Susan Parker is a highly experienced individual with a background in coordinating phase 1, 2, and 3 trials, surveillance, and anti-viral treatment studies. She excels in writing protocols, IRB proposals, informed consent documents, and various clinical study materials. Susan's expertise includes collecting and processing clinical specimens, administering study products, and developing quality management tools. With a Bachelor's degree in research methodology and a background as a Registered Nurse, Susan has specialized in protocol development, informed consent writing, and quality management.

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Location

Cincinnati, Ohio, United States