A dedicated pharmaceutical professional with the strong knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, GMP, and GCP. Specialized in clinical pharmacology, psychopharmacology, quality control, and management of clinical trial. Strongly Proficient in complying with study protocols, standard operating procedures and good clinical practices. Practiced problem-solver with strong attention to detail. Prepared to offer 4 years' experience in the field and take on a fast-paced position.
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