Analyst-Dose Analysis Sign On Bonus Available

<h2>Job Overview:</h2><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;"><strong>Labcorp Drug Development </strong>is currently hiring for a <strong><em>Analyst</em></strong> to join our Dose Analysis team in Somerset, New Jersey.  </span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Responsibilities of a Analyst include (but are not limited to):</span></p><p style="margin: 0px;"> </p><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Organizes and conducts routine analyses in compliance with applicable methods, protocols, SOPs, and regulatory agency guidelines.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Documents work and maintains study documentation and laboratory records.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Sets up, operates and performs routine and non-routine maintenance on general equipment.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Provides input and participates in project meetings, plans, monitors and guides project work.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Performs QC review of data.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Informs Study Director, Principal Investigator and/or management of any problems and/or deviations that may affect the integrity of the data and participates in corrective action of problems.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Assists in setting up and performing method development and validation of various analytes in a variety of matrices.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Maintains a clean and safe laboratory work environment.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Contributes towards a cohesive team environment.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Participates in process improvement initiatives.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Evaluates data for report preparation and experiment modification as directed.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Plans individual workload in coordination with team members.</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Assists in writing text for reports, methods or protocols. </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Performs other related duties as assigned</span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 10.0pt; font-family: 'Arial',sans-serif;">BA/BS degree or above in Life Sciences, Chemistry or related plus minimum 1 to 2 years of laboratory</span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Good communication, time management, organizational and attention to details skills. </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Good understanding of pharmaceutical industry and Good Laboratory Practice (GLP).</span></li></ul><h2>Experience:</h2><ul><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">General laboratory and routine sample analysis experience is required by HPLC and GC. </span></li><li><span style="font-family: arial, helvetica, sans-serif; font-size: 10pt;">Solid computer skills.</span></li></ul>