Senior Study Manager - Residue Analysis - Excellent progression opportunity!

<h2>Job Overview:</h2><p style="margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Are you looking for a role that will expand your career in Analytical Chemistry?</strong></span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Do you have the skills and experience to liaise with clients on a variety of studies?</strong></span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>Do you want to work for a Scientific company that is a world leader in Pharmaceutical and Environmental development?</strong></span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">This is to undertake the role of<strong> Study Manager / Analytical Principal Investigator</strong> for assigned studies.  Responsible for the supervision and reporting of assigned work to ensure that all analytical studies are performed to satisfactory scientific standards, in accordance with Study Plan, GLP and relevant SOPs. </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: black;">These studies can be carried out on a variety of samples such as fruit, vegetables, soil, air, water and biological samples. </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong>As a Study Manager your responsibilities will be:</strong></span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;"> </span></p><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">To ensure that the agreed timelines are consistent with the Sponsors needs and/or agreed company start up times.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Monitor the status of observations made during the study and ensure the responses are fully documented.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">To review all data to ensure its accuracy.  To ensure that the study is compliant with Good Laboratory Practice and that suitable responses/actions are made following Quality Assurance Audit.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">To be aware of the study status, anticipate problems that may affect the schedule date, purpose or integrity of the study.  </span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">To inform the Sponsor of the results as soon as possible after the study completion date.  To prepare draft and final reports ensuring the report is concisely and accurately written, reflects the raw data and includes all relevant information.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">To maintain the computerised monitoring system for studies such that the information is up to date to enable study monitoring by their supervisors and other departments such as Quality Assurance.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Where appropriate co-ordinating the supply of test materials, test vessels and equipment in conjunction with other members of staff thereby ensuring their availability for study start up.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Being aware of all experimental equipment in use and ensuring that all technicians are adequately trained in its use.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">Train and supervise staff.</span></li></ul><p style="margin-left: .25in;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif;">                 </span></p><p style="margin: 0px;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;"><strong><span style="color: #0a0a0a;">We Offer:</span></strong></span></p><p style="margin: 0px;"> </p><p style="margin: 0px;"> </p><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #0a0a0a;">Covance by Labcorp offers a comprehensive benefits package, including health cover and contributory pension.</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #0a0a0a;">A relocation package (subject to guidelines).</span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #0a0a0a;">Covance by Labcorp's ongoing success offers team members unsurpassed growth and career development opportunities. </span></li><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #0a0a0a;">We will support your professional development every step of the way!</span></li></ul><p style="margin-left: 18.0pt;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt;">                </span></p><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: black;">Advanced degree (e.g. MSc/PhD) with industry experience preferred (BSc. minimum with extensive direct industry experience)</span></li></ul><h2>Experience:</h2><ul><li style="text-align: justify;"><span style="font-size: 12pt; font-family: arial, helvetica, sans-serif; color: #000000;">Experience working as a Study Director with a knowledge and understanding of GLP regulations.</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Skilled in performing scientific presentations and preparing scientific publications.</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Excellent attention to detail, methods and interpretation of scientific data.</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Previous experience of client management skills and technical expertise in the relevant business line is preferable.</span></li><li style="text-align: justify;"><span style="font-family: arial, helvetica, sans-serif; font-size: 12pt; color: #000000;">Excellent communication (verbal and written), teamwork and interpersonal skills.</span></li></ul>