Ryan Turncliff

Background

About Ryan Turncliff

Clinical Drug Developer with 20+ years of pharmaceutical drug discovery and development experience in pharma and CRO realms. Strong theoretical background in clinical pharmacology supports hands-on experience designing, conducting/outsourcing, analyzing and reporting clinical trials. Current regulatory experience with application of modeling & simulation within early and late-stage projects (eg: MIDD). Extensive in vivo/in vitro ADME and nonclinical tox knowledge. History of success in CNS drug development. Late stage develop projects in Oncology and CNS as well as support and conduct of BE studies across multiple therapeutic areas. Experienced in global clinical study conduct including Asia (India) and LATAM regions. Comprehensive first hand-regulatory experience, from IND authoring through NDA submission, FDA Advisory Committee meeting and approval/labeling. Management experience and departmental fiduciary accountability; responsible selection of outsourced partner selection. Demonstrated strategic leadership, excellent communication and organization savvy, combined with strong business acumen, hands-on approach and a collaborative “can do” attitude.