Study Director - Cell & Gene Therapy

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: black;">Looking for a career that will make an impact on patient lives? Come join a <strong><span style="font-family: 'Arial',sans-serif;">global leader</span></strong> in drug development!  We have a great opportunity for a </span><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: blue;">STUDY DIRECTOR </span></strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">specializing in <strong><span style="font-family: 'Arial',sans-serif;">Cell & Gene Therapy</span></strong> to join our preclinical Study Direction team <span style="color: black;">at our Madison, WI site.  Covance’s work in developing new pharmaceutical solutions has an incredible impact on the lives of millions worldwide.  Be a part of this life-saving work.</span></span></p><p style="margin: 0px;"> </p><p style="margin-bottom: .0001pt;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: blue;">In this role, you will:</span></strong></p><ul><li style="margin-left: 1.0in;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Serves as the scientific specialist for the Cell & Gene Therapy specialty program and serves as a Study Director for studies, as described in GLPs. </span></li><li style="margin-left: 1.0in;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Has overall responsibility for the technical conduct of a study, as well as for the interpretation, analysis, documentation, and reporting of results.</span></li><li style="margin-left: 1.0in;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">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 and play a key role in developing new strategies, techniques, and instrumentation for new ventures and critical issues in the area of specialty.</span></li></ul><p style="margin-bottom: .0001pt;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: blue;">What we’re looking for in you:</span></strong></p><ul><li style="margin-left: 1.0in;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Has aPhD, DVM, or equivalent degree;</span></li><li style="margin-left: 1.0in;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">3-5 years experience in Regenerative Medicine, Transplantation, and/or Virology</span></li><li style="margin-left: 1.0in;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Maintains current regulatory awareness (domestic and foreign);</span></li><li style="margin-left: 1.0in;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Is skilled in performing scientific presentations and preparing scientific publications;</span></li><li style="margin-left: 1.0in;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Is recognized by research peers as an expert in a selected technical field;</span></li><li style="margin-left: 1.0in;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">In addition, DABT certification is desirable.</span></li></ul><p style="margin-bottom: .0001pt;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif; color: blue;">There is no better time to join us!</span></strong></p><p style="margin-bottom: .0001pt;"><span style="color: #ffffff;"><strong><span style="font-size: 12pt; font-family: Arial, sans-serif;">#LI-TC1</span></strong></span></p><h2>Education/Qualifications:</h2><p style="margin: 0px;"><span style="font-size: 11.0pt;">PhD in toxicology or related field preferred, BSc or MSc or equivalent degree in toxicology or related field.  Experience Relevant experience may be substituted for years of related experience.</span></p><p style="margin: 0px;"><span style="font-size: 11.0pt;">Board certification in toxicology is desired. Home Office License desired (if appropriate).</span></p><h2>Experience:</h2><ul><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">3 to five years of safety assessment study direction experience and drug development experience</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Highly skilled in conducting research, data interpretation, and writing reports.</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Highly skilled in performing scientific presentation and preparing scientific publications</span></li><li style="margin-left: .5in;"><span style="font-size: 11.0pt;">Knowledge and/or experience in drug development field.</span></li></ul>