Coord Reg Submissions

<h2>Job Overview:</h2><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;">Individual Contributor</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Under the direction of senior staff, assist with the formatting and compilation of regulatory</span></span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;">submissions through such tasks as entering information into Tables of Contents and creating</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;">tabs and submission labels.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Provide support assistance to senior staff in the upkeep of regulatory authority submission and</span></span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;">correspondence logs (add entries to Tables of Contents, file submission letters and other</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;">correspondence).</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Generate routine submission cover letters to regulatory authorities and clients.</span></span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Track, inventory and organize individual components of regulatory submissions.</span></span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Perform document acceptability checks of submission components.</span></span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Liaise with the Publishing group in the generation of submissions.</span></span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Provide support assistance to senior staff in the oversight, final preparation and generation of</span></span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;">submission documents.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Perform a quality check of final submission documents.</span></span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Update status reports and tracking sheets of ongoing and pending regulatory projects with input</span></span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;">provided by senior staff.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Organise shipping of documentation to clients, regulatory authorities and within Covance.</span></span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Perform other job functions, such as word processing, as needed to accomplish the above listed</span></span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;">duties.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 12pt;"><span style="font-family: Symbol;">¨ </span><span style="font-family: Times-Roman, serif;">Perform other activities as required by management</span><span style="font-family: 'Times-Roman',serif;">.</span></span></p><h2>Education/Qualifications:</h2><p style="margin: 0px;"><span style="font-size: 12pt;">Bachelor’s Degree in Life Sciences or equivalent (new Graduates are welcome)</span></p><h2>Experience:</h2><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 13.5pt; font-family: Symbol;">¨ </span><span style="font-size: 13.5pt; font-family: 'Times-Roman',serif;">Excellent verbal and written communication skills.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 13.5pt; font-family: Symbol;">¨ </span><span style="font-size: 13.5pt; font-family: 'Times-Roman',serif;">Computer literacy in basic functions (Word, Excel)</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 13.5pt; font-family: Symbol;">¨ </span><span style="font-size: 13.5pt; font-family: 'Times-Roman',serif;">Good planning and organizational skills; detail oriented.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 13.5pt; font-family: Symbol;">¨ </span><span style="font-size: 13.5pt; font-family: 'Times-Roman',serif;">Flexibility, ability to switch back and forth between multiple projects/tasks.</span></p><p style="margin: 0in; margin-bottom: .0001pt;"><span style="font-size: 13.5pt; font-family: Symbol;">¨ </span><span style="font-size: 13.5pt; font-family: 'Times-Roman',serif;">Understanding/knowledge of drug regulations</span></p>