Senior Study Director - Metabolism

<h2>Job Overview:</h2><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Our team is growing! We are looking to add a <strong>Senior</strong> <strong>In Vitro </strong><strong>Study Director</strong> to our Drug Metabolism team in Madison, WI. The Study Director is responsible for managing the design, conduct and reporting of studies to meet scientific, regulatory and client requirements.  The Study Director is the single point of study control and has overall responsibility for the scientific, technical and regulatory conduct of studies as well as for the interpretation, documentation and reporting of results. Close and regular liaison with the client is of primary importance.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"> </span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">The Study Director will demonstrate competence in directing studies of intermediate complexity in design and scope. The majority of studies undertaken will be non-GLP studies and routine & more complex GLP, GCP or GMP studies.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"> </p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">With two state-of-the-art metabolism laboratories in Madison, Wisconsin, and Harrogate, UK, Covance has helped hundreds of pharmaceutical and biotechnology companies select compounds to progress into development. Covance provides a comprehensive range of ADME services to support drug discovery and development programs.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"> </p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">At Covance by Labcorp, you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. Our commitment to this mission has resulted in an impressive history of company stability and growth. We’ve achieved these results by fostering a work environment that encourages, develops and leverages our team’s capabilities.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"> </p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Come join a global leader in drug development.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Patients can't wait.  Neither can we.</span></p><p style="margin: 0px;"><span style="color: #ffffff;">#LI-TC1</span></p><h2>Education/Qualifications:</h2><p style="margin: 0px;"><span style="font-size: 11.0pt; font-family: 'Times New Roman',serif;">PhD or experience may be substituted for education.</span></p><h2>Experience:</h2><p style="margin: 0px;"><span style="font-size: 11.0pt; font-family: 'Times New Roman',serif;">5-7 years of relevant experience</span></p>