Reporting Associate - Safety Assessment (Madison, WI)

<h2>Job Overview:</h2><p style="margin-bottom: 6.75pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Do you have a passion for Science? Report Writing? Customer Relations? Accuracy? Please keep reading…</span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">We are currently recruiting for a Reporting Associate to join Covance by Labcorp for our office-based position in Madison, WI. During the current pandemic, this position is a work from home position with minimal onsite tasks. This is an exciting opportunity that will offer you the chance to become part of an exceptionally talented staff community that helps to bring the miracle of medicine to the market sooner.</span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;"> </span></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><h2>Education/Qualifications:</h2><ul><li style="font-family: Arial; font-size: 12pt; color: #333333;"><span style="font-family: Arial; font-size: 12.0pt; color: #333333;">Preferred: Degree and/or experience in science, technical writing, and/or document production/publishing</span></li><li style="font-family: Arial; font-size: 12pt; color: #333333;"><span style="font-family: Arial; font-size: 12.0pt; color: #333333;">Bachelor’s degree in Biology or related field and/or equivalent experience.</span></li></ul><h2>Experience:</h2><ul><li><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><span style="font-family: Arial; font-size: 12.0pt; color: #333333;">Attention to detail, time management skills, and organizational skills</span></li><li><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>