Reporting Associate Developmental and Reproductive Toxicology team

<h2>Job Overview:</h2><p style="margin: 0px; text-align: center;"><strong><span style="font-family: 'times new roman', times; font-size: 12pt;">Reporting Associate in our Developmental and Reproductive Toxicology (DART</span></strong></p><p style="margin: 0px; text-align: center;"><strong><span style="font-family: 'times new roman', times; font-size: 12pt;">Greenfield, Indiana </span></strong></p><p style="margin: 0px;"> </p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: 'times new roman', times;">We are currently recruiting for a <strong>Reporting Associate in our Developmental and Reproductive Toxicology (DART) team to join the Labcorp Drug Development position in Greenfield.</strong> During the current pandemic, this position is a work from home position with minimal on-site 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: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: 'times new roman', times;">By joining us you can make a difference by helping to deliver life-saving and life-enhancing medicines to people around the world. </span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: 'times new roman', times;">The <strong>Reporting Associate II</strong> is 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 II, you will utilize your scientific knowledge while working independently to deliver signature client service to our customers. Once fully trained you will manage a full study workload with complex study designs by adhering to report preparation schedules and prioritizing tasks. Identifies and resolves changes to established study schedules to ensure client deliverables are met. Additional duties include but not limited to;</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: 'times new roman', times;"><strong>Report Preparation</strong> according to the study report using details described in the protocol, protocol amendments, and study communications and Labcorp Drug Development or client-specific requirements. Will incorporates contributions (e.g., protocol, protocol amendments, certificates of analysis, contributor reports) into the draft report. May address quality assurance inspection items on GLP (Good Laboratory Practice) regulated studies. Finalizes study reports and obtain, prepare, and deliver materials to archives, may prepare report amendments. May assist in the preparation of tabulated summaries in association with the study director. Will prepares data tables including completing basic statistical analysis in table generation programs.</span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: 'times new roman', times;"><strong>Scheduling Responsibilities</strong> will review and adjust the reporting schedule to ensure client expectations are met. May lead the prewriting meeting, as required. Will schedule and coordinate study report finalization efforts. May coordinate expedited reporting, as necessary, among global counterparts</span></p><p style="margin: 0px;"><br /><span style="font-size: 12pt; font-family: 'times new roman', times;"><strong>Client interaction</strong> will prepare form letters and communications for clients. May coordinate client on-site meetings and conference and video calls. May respond to client inquiries for information and updates.</span> </p><h2>Education/Qualifications:</h2><p style="margin: 0px;"><span style="font-size: 12pt; font-family: 'times new roman', times;">Preferred but not required, Bachelor's Degree in life Science such as Biology or related science. Equivalent experience may be used in lieu of education. Helpful but not required is experience in science, technical writing, and/or document production/publishing</span><br /><span style="font-size: 12pt; font-family: 'times new roman', times;">Prior experience with DART (Development and Reproductive Toxicology Studies) is helpful but not required</span></p><p style="margin: 0px;"> </p><h2>Experience:</h2><p style="margin: 0px;"><span style="font-size: 12pt; font-family: 'times new roman', times;">One or more years of related Toxicology, Animal Research or Preclinical Drug Studies is preferred but not required. One or more years of working in a CRO (Contract Research Organization) is preferred but not required. Excellent keyboarding skills with good knowledge of office software (e.g., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)</span><br /><span style="font-size: 12pt; font-family: 'times new roman', times;">Attention to detail, time management skills, and organizational skills. Preferred but not required is one year of reporting, technical writing or data tabulation experience in a </span><br /><span style="font-size: 12pt; font-family: 'times new roman', times;">n pharmaceutical research or life sciences area.</span> </p>