Reporting Associate - Safety Assessment

<h2>Job Overview:</h2><p style="margin-bottom: 6.75pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><span style="color: #333333;">Do you have a passion for Science? Report Writing? Customer Relations? Accuracy?</span></span></p><p style="margin-bottom: 6.75pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: black;">We have a great opportunity for a Reporting Associate in our Safety Assessment Department at our Madison, WI lab. </span><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: black;">Labcorp Drug Development's work in developing new pharmaceutical solutions has an incredible impact on millions of lives worldwide. Be a part of this life-saving work and help improve patients' lives while growing your career.</span></p><p style="margin-bottom: 6.75pt;"><strong><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;"><span style="color: #000000;">We are offering a sign-on bonus of $3,000 ($1,500 upon hire and $1,500 after 6 months).</span></span></strong></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: black;">In this role, you will be responsible for generating data tables, drafting scientific reports, maintaining professional relationships with clients, communicating with internal staff, and working independently on projects. The ideal candidate will possess skills in time management, organization, and project management. As a Reporting Associate, you will utilize your scientific knowledge while working independently to deliver signature client service to our customers. Also, you will learn and perform the duties of drafting and finalizing nonclinical scientific study reports.</span></p><p style="margin-bottom: .0001pt;"> </p><p style="margin-bottom: 10.0pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">The Reporting Associate  is responsible for communication between internal teams and clients, will coordinate and provide status updates to deliverables, generating data tables, drafting scientific reports, and working independently on projects.  Duties include but not limited to:</span></p><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Drafts and prepares communication to client and internal stake holders including regular contact with clients </span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;">Prepares and finalizes study reports according to study protocol, amendments and client specific requirements </span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;">Prepares complex data tables including the use of statistical analysis and table generation programs </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Addresses quality assurance inspection items on GLP-regulated studies </span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;">Coordinates the study deliverables ensuring items are completed by prescribed timeline including coordination among global counterparts   </span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;">Identifies and resolves changes to established study schedules to ensure client deliverables are met</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Prepares final study documents; may print, bind and prepare for final delivery</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Prepares tabulated summaries in association with the study director</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;">Schedules and leads prewriting meetings</span></li></ul><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">In this position you can apply your scientific knowledge from preclincal studies in preparing and coordination of reporting and deliverables.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;"><span style="font-size: 8pt;">#LI-DZ1</span></span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;"><span style="font-size: 8pt;">#T1RB</span></span></p><h2>Education/Qualifications:</h2><ul><li><span style="font-family: Arial; font-size: 12.0pt; color: #333333;">Degree and/or experience in science (Biology, Animal Science, etc.), technical writing, and/or document production/publishing </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Work experience may be a substitute for education. </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">Strong oral and written communication skills </span></li></ul><h2>Experience:</h2><ul><li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;"><span style="font-family: Arial; font-size: 12.0pt; color: #333333;">Basic knowledge of office software (e.g., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)</span></li><li style="margin-top: 0; margin-bottom: 0; vertical-align: middle;"><span style="font-family: Arial; font-size: 12.0pt; color: #333333;">Attention to detail, time management skills, and organizational skills</span></li><li style="margin-top: 0pt; margin-bottom: 10pt; vertical-align: middle;"><span style="font-family: Arial; font-size: 12.0pt; color: #333333;">Prefer at least 1 year of technical writing or data tabulation experience, especially in pharmaceutical research or life sciences.</span></li></ul>