full-time part-time employee contract
Job Overview:Covance’s work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide. Be a part of this life-saving work. We have a unique opportunity for a Study Director in our Safety Pharmacology team in Madison, WI.This role:Serves as the scientific specialist on GLP-compliant cardiovascular, central nervous system, and/or respiratory safety pharmacology studies.Opportunity for designing and conducting fit-for-purpose studies for test article hazard identification/characterization. Has overall responsibility for the technical conduct of a study, as well as for the interpretation, analysis, documentation, and reporting of results.Assists or may plan, design, and/or lead a team to conduct complex studies to generate high quality scientific results on behalf of Covance clients. Plays a key role in developing new strategies, techniques, and instrumentation for new ventures and critical issues in the area of specialty.Experience with large and small animal echocardiography a plus. What we’re looking for in you:PhD in pharmacology, toxicology, physiology or related subject; DVM or equivalent degree may also suffice. Experience may be substituted for education. DSP or DABT certification is preferred.There is no better time to join us! #LI-TC1 Education/Qualifications:Required:PhD in pharmacology, toxicology, physiology or related subject; DVM or equivalent degree may also suffice. Experience may be substituted for education. DSP or DABT certification is preferred.Experience:Minimum Required:Zero to two years of related experience.Skilled in performing scientific presentations and preparing technical reports and original scientific publications.