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Tanji Goodfellow joined Lifetree Clinical Research® in June 2007. Goodfellow has over 23 years experience in the clinical research industry and has personally been involved with five new drug application approvals and numerous Food and Drug Administration (FDA) audits. Prior to joining the Lifetree Clinical Research® team, she was director of clinical operations at Cadence Pharmaceuticals in San Diego, Calif. where she was responsible for planning, execution and conduct of clinical research operations to ensure compliance with FDA regulations, established guidelines from the International Conference on Harmonization, and good clinical practice (GCP) guidelines. She has experience in the writing and development of clinical standard operating procedures, oversight of GCP training requirements for company staff and development, and execution of GCP audit plans for numerous clinical development programs.Goodfellow has also worked for Biogen Idec Pharmaceuticals in San Diego, Calif., NovoNordisk Pharmaceuticals in Princeton, N.J., and for Anesta Corp, IOMED and Symbion in Salt Lake City, Utah. | 