Pathology Assistant Reporting Specialist

<h2>Job Overview:</h2><p style="margin: 0px; text-align: center;"><span style="font-size: 14pt;"><strong><span style="font-family: 'times new roman', times;">Pathology Assistant Reporting Specialist</span></strong></span><br /><span style="font-size: 14pt;"><strong><span style="font-family: 'times new roman', times;">Greenfield Indiana </span></strong></span><br /><br /><span style="font-family: 'times new roman', times; font-size: 12pt;">Do you have a background in <strong>Laboratory Pathology, Animal Research studies or Toxicology and passion for Quality Control (QC) and reporting? If so, the Pathology Assistant -Reporting Specialist</strong> may be the next career step for you! In this position you will put your knowledge and skills in Pathology, Animal Research or Toxicology while working closely with Scientists, Principal Investigators and Pathologists in the production of pathology reports for research studies. </span><br /><br /><span style="font-family: 'times new roman', times; font-size: 12pt;">The ideal candidate has strong knowledge in Pathology, Animal Research studies or Toxicology in order to interpret data to confirm it meets the study protocol and regulatory requirements, perform quality control (QC) and translate data into standardized reporting format. We are also seeking candidates that have a proven record in prioritizing and delivering upon multiple competing deadlines all while maintaining the accuracy and standards of the data. Other duties include but not limited to;</span></p><ul><li style="text-align: left;"><span style="font-family: 'times new roman', times; font-size: 12pt;">Responsible for assisting pathologists and related staff on the technical aspects of the histopathologic evaluation and reporting of the study.</span></li><li style="text-align: left;"><span style="font-family: 'times new roman', times; font-size: 12pt;">Provide QC review of pathologist-generated data for completeness and accuracy to the report, to the protocol-requirements, to applicable SOPs, and/or departmental procedures</span></li><li style="text-align: left;"><span style="font-family: 'times new roman', times; font-size: 12pt;">Receive, update, and help pathologists maintain version control of pathology reports due to revisions from clients, peer review pathologists, study direction, etc.</span></li><li style="text-align: left;"><span style="font-family: 'times new roman', times; font-size: 12pt;">Generating the of anatomic pathology report tables from applicable data collection/reporting systems (e.g. Toxicology Reporting) for inclusion in anatomic pathology reports</span></li><li style="text-align: left;"><span style="font-family: 'times new roman', times; font-size: 12pt;">Advise on pathology report structure for reader-clarity</span></li><li style="text-align: left;"><span style="font-family: 'times new roman', times; font-size: 12pt;">Respond to quality assurance inspections and study communications</span></li><li style="text-align: left;"><span style="font-family: 'times new roman', times; font-size: 12pt;">Work and communicate closely with study team to ensure the appropriate protocol requirements are met and participate in study-related meetings, as required</span></li><li style="text-align: left;"><span style="font-family: 'times new roman', times; font-size: 12pt;">May aid in preparation for on-site client peer reviews including meeting planning and organization, preparing peer review data packets, creating and delivering slide presentations.</span></li></ul><p style="margin: 0px;"> </p><h2>Education/Qualifications:</h2><p style="margin: 0px;"><span style="font-size: 12pt; font-family: 'times new roman', times;">Bachelor’s degree in life science or related field or equivalent experience.</span><br /><span style="font-size: 12pt; font-family: 'times new roman', times;">Knowledge of laboratory equipment and procedures and awareness of quality control and calibration.</span><br /><span style="font-size: 12pt; font-family: 'times new roman', times;">Prior experience in producing scientific reporting, technical writing, document production/publishing, and/or science preferred but not required.</span></p><h2>Experience:</h2><p style="margin: 0px;"><span style="font-family: 'times new roman', times; font-size: 12pt;">2+ years of experience in toxicology, animal research, Contract Research Organization (CRO) or clinical laboratory experience. </span><br /><span style="font-family: 'times new roman', times; font-size: 12pt;">Prior experience with pristima or other helpful laboratory management software is helpful but not required.</span><br /><span style="font-family: 'times new roman', times; font-size: 12pt;">Prior experience/knowledge of GLP (Good Laboratory Practice) studies and applicable regulatory requirements is desired.</span><br /><span style="font-family: 'times new roman', times; font-size: 12pt;">Strong software skills to create, edit and deliver complex data reporting </span><br /><span style="font-family: 'times new roman', times; font-size: 12pt;">Excellent organizational skills; ability to prioritize workload and problem solve with little or no direct supervision is desired</span></p>