Salary: $110,000 to $150,000
Contact: Nikki Quist, Nquist@smithhanley.com
"Provide statistical input to the design, analysis, reporting and interpretation of clinical studies.
"Provide clinical development plans, regulatory and commercial strategies.
"Build and maintain strategic working relationships
"Identify, develop, and implement novel statistical methodologies
"PhD or MS in Biostatistics, Statistics or related field
"5 + years experience in the design, execution, analysis and interpretation of clinical trials.
"Expertise in statistical methodologies.
"Experience with pharmacokinetic and pharmacodynamics (i.e., biomarker)
"Linear as well as nonlinear dose response modelling is a plus.
"Leadership capabilities in support and management of a wide variety of tasks across projects.
"Excellent communication skills.
"Solid understanding of drug development processes and strategies.
"Experience supporting product life-cycle management.
" Experience providing support for publications
"Experience in submissions
" Experience of working with CROs.
Experience with modeling and simulation and other methodologies