San Diego, CA30+ days ago
Experience as a clinical scientist responsible for data review, safety monitoring, protocol development, supporting data analyses, interpretation and publications also required, as well as clinical research experience in area of focus, strong, hands-on working knowledge of drug development, and experience working on cross functional clinical trial teams and liaising with study investigators. Education/Experience/Skills: Position requires a BS degree in life sciences; PhD, RN, PharmD or MS preferred and a minimum of 15 years of directly relevant pharmaceutical industry experience in clinical development and a minimum of 4 years' experience of focus in assigned therapeutic area.