Scientific Administrator - Genetic Toxicology

<h2>Job Overview:</h2><p style="margin: 0px;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Do you have an interest in science but don’t want to work in the laboratory?</span></strong></p><p style="margin: 0px;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></strong></p><p style="margin: 0px;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Do you have excellent attention to detail, organizational and communication skills?</span></strong></p><p style="margin: 0px;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></strong></p><p style="margin: 0px;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Are you looking for a looking for a role where you can impact on improving lives and improving health?</span></strong></p><p style="margin: 0px;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin: 0px;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Labcorp is a leading global life sciences company that includes contract research and developmental services to the pharmaceutical, medical technology, crop protection and chemical industries.</span></p><p style="margin: 0px;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin: 0px;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">We are currently recruiting for a Scientific Administrator to join us at an entry level position in the Genetic Toxicology group located in Huntingdon, Cambridgeshire. As a Scientific Administrator, you will learn the tasks required to support the drafting of study reports, format checking and preparation of protocols and reports, to distributing these internally and externally according to agreed schedules and requirements. You will also perform other administrative tasks relating to Genetic Toxicology, as required.</span></p><p style="margin: 0px;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin: 0px;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Report Drafting:</span></strong></p><p style="margin: 0px;"> </p><ul style="margin-top: 0in;"><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Using information from the protocol and study files, prepare study reports for the Study Director containing factual information and study data. </span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Liaise with the Study Director to discuss details of the study and any special requirements for the report.</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Prepare, format and check reports to the scheduled deadlines according to Covance or client-specific requirements.</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Prepare and quality check tabulated summaries </span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Assist Study Director in addressing quality assurance inspection items on GLP-regulated studies, as required.</span></li></ul><p style="margin: 0px;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin: 0px;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Study Support:</span></strong></p><ul><li><span style="font-family: Arial, sans-serif; font-size: 12pt;">Prepare and format check study protocols and reports to individual client requirements prior to Quality Assurance audit and dispatch to the client.</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Prepare and format check reports for finalisation (including adding contributory reports, signatures etc).</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Archive raw study data and final reports.</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Assist in maintenance of site-specific protocol and report templates</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Complete and maintain databases and spreadsheets.</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">General support as required.</span></li></ul><p style="margin: 0px;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin: 0px;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Other responsibilities may include:</span></strong></p><p style="margin: 0px;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></strong></p><ul><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Ordering of stock and external items.</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Maintaining/updating relevant departmental spreadsheets.</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">General administrative tasks as assigned, which may include distribution of post and form production and issue.</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Assisting with travel arrangements, making internal bookings as required/ requested.</span></li></ul><p style="margin: 0px;"><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;"> </span></p><p style="margin: 0px;"><strong><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">What Labcorp Drug Development can offer you:</span></strong></p><ul><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Competitive salaries and a comprehensive benefits package including health cover and contributory pension.</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Unrivalled opportunities to develop a successful career in the scientific industry.</span></li><li><span style="font-size: 12.0pt; font-family: 'Arial',sans-serif;">Unsurpassed career development opportunities.</span></li></ul><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">If you are looking for a role where you will receive first class training, then we would like to hear from you!</span></p><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">A Levels in English / related subject or equivalent experience. </span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">A levels /or experience in technical writing, document production/publishing</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Basic knowledge of office software (e.g., Microsoft® Office, especially Word and Excel; Adobe® Acrobat®)</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Excellent attention to detail, time management skills, and organisational skills</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Excellent communication, presentation and interpersonal skills.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Ability to prioritise workload and work to deadlines</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">An intereest and/or experience in science is advantageous but not essential</span></li></ul>